NDC 0078-0569 Extavia

Interferon Beta-1b

NDC Product Code 0078-0569

NDC 0078-0569-12

Package Description: 15 BLISTER PACK in 1 CARTON > 1 KIT in 1 BLISTER PACK (0078-0569-61) * 3 mL in 1 VIAL, SINGLE-USE * 1.2 mL in 1 SYRINGE

NDC Product Information

Extavia with NDC 0078-0569 is a a human prescription drug product labeled by Novartis Pharmaceuticals Corporation. The generic name of Extavia is interferon beta-1b. The product's dosage form is kit and is administered via form.

Labeler Name: Novartis Pharmaceuticals Corporation

Dosage Form: Kit - A packaged collection of related material.

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Inactive Ingredient(s)

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Product Labeler Information

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Labeler Name: Novartis Pharmaceuticals Corporation
Labeler Code: 0078
FDA Application Number: BLA125290 What is the FDA Application Number?
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Marketing Category: BLA - A product marketed under an approved Biologic License Application. What is the Marketing Category?
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Start Marketing Date: 08-14-2009 What is the Start Marketing Date?
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Listing Expiration Date: 12-31-2021 What is the Listing Expiration Date?
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Exclude Flag: N What is the NDC Exclude Flag?
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Information for Patients

Interferon Beta-1b Injection

Interferon Beta-1b Injection is pronounced as (in" ter feer' on bay' ta wun bee)

Why is interferon beta-1b injection medication prescribed?
Interferon beta-1b injection is used to reduce episodes of symptoms in patients with relapsing-remitting (course of disease where symptoms flare up from time to time) of ...
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Extavia Product Labeling Information

The product labeling information includes all published material associated to a drug. Product labeling documents include information like generic names, active ingredients, ingredient strength dosage, routes of administration, appearance, usage, warnings, inactive ingredients, etc.

Product Labeling Index

1     Indications And Usage

EXTAVIA (interferon beta-1b) is indicated for the treatment of relapsing forms of multiple sclerosis to reduce the frequency of clinical exacerbations. Patients with multiple sclerosis in whom efficacy has been demonstrated include patients who have experienced a first clinical episode and have MRI features consistent with multiple sclerosis.

2.1     Dosing Information

The recommended starting dose is 0.0625 mg (0.25 mL) subcutaneously every other day, with dose increases over a six-week period to the recommended dose of 0.25 mg (1 mL) every other day (see Table 1).Table 1: Schedule for Dose Titration1 Dosed every other day, subcutaneouslyEXTAVIADose1Percentage ofrecommended doseVolumeWeeks 1-20.0625 mg25%0.25 mLWeeks 3-40.125 mg50%0.5 mLWeeks 5-60.1875 mg75%0.75 mLWeek 7 and thereafter0.25 mg100%1 mLIf a dose of EXTAVIA is missed, then it should be taken as soon as the patient remembers or is able to take it. The patient should not take EXTAVIA on two consecutive days. The next injection should be taken about 48 hours (two days) after that dose. If the patient accidentally takes more than their prescribed dose, or takes it on two consecutive days, they should be instructed to call their healthcare provider immediately.

2.2     Reconstitution Of The Lyophilized Powder

(a) Prior to reconstitution, verify that the vial containing lyophilized EXTAVIA is not cracked or damaged. Do not use cracked or damaged vials.(b) To reconstitute lyophilized EXTAVIA for injection, attach the pre-filled syringe containing the diluent (Sodium Chloride, 0.54% Solution) to the EXTAVIA vial using the vial adapter. The removable rubber cap of the diluent (Sodium Chloride, 0.54% Solution) pre-filled syringe contains natural rubber latex, which may cause allergic reactions and should not be handled by latex-sensitive individuals.(c) Slowly inject 1.2 mL of diluent into the EXTAVIA vial. (d) Gently swirl the vial to dissolve the lyophilized powder completely; do not shake. Foaming may occur during reconstitution or if the vial is swirled or shaken too vigorously. If foaming occurs, allow the vial to sit undisturbed until the foam settles. (e) 1 mL of reconstituted EXTAVIA solution contains 0.25 mg of interferon beta-1b.(f) After reconstitution, if not used immediately, refrigerate the reconstituted EXTAVIA solution at 35°F to 46°F (2°C to 8°C) and use within three hours. Do not freeze.

2.3     Important Administration Instructions

(a) Perform the first EXTAVIA injection under the supervision of an appropriately qualified healthcare professional. If patients or caregivers are to administer EXTAVIA, train them in the proper subcutaneous injection technique and assess their ability to inject subcutaneously to ensure the proper administration of EXTAVIA. (b) Visually inspect the reconstituted EXTAVIA solution before use; discard if it contains particulate matter or is discolored. (c) Keeping the syringe and vial adapter in place, turn the assembly over so that the vial is on top. Withdraw the appropriate dose of EXTAVIA solution. Remove the vial from the vial adapter before injecting EXTAVIA. (d) Use safe disposal procedures for needles and syringes. (e) Do not re-use needles or syringes.(f) Advise patients and caregivers to rotate sites for subcutaneous injections to minimize the likelihood of severe injection site reactions, including necrosis or localized infection.

2.4     Premedication For Flu-Like Symptoms

Concurrent use of analgesics and/or antipyretics on treatment days may help ameliorate flu-like symptoms associated with EXTAVIA use [see Warnings and Precautions (5.8)].

3     Dosage Forms And Strengths

For injection: 0.3 mg lyophilized powder in a single-use vial for reconstitution.

4     Contraindications

EXTAVIA is contraindicated in patients with a history of hypersensitivity to natural or recombinant interferon beta, Albumin (Human), or any other component of the formulation.

5.1     Hepatic Injury

Severe hepatic injury including cases of hepatic failure, some of which have been due to autoimmune hepatitis, has been rarely reported in patients taking EXTAVIA. In some cases, these events have occurred in the presence of other drugs or comorbid medical conditions that have been associated with hepatic injury. Consider the potential risk of EXTAVIA used in combination with known hepatotoxic drugs or other products (e.g., alcohol) prior to EXTAVIA administration, or when adding new agents to the regimen of patients already on EXTAVIA. Monitor patients for signs and symptoms of hepatic injury. Consider discontinuing EXTAVIA if serum transaminase levels significantly increase, or if they are associated with clinical symptoms such as jaundice.Asymptomatic elevation of serum transaminases is common in patients treated with EXTAVIA. In controlled clinical trials, elevations of SGPT to greater than five times baseline value were reported in 12% of patients receiving interferon beta-1b (compared to 4% on placebo), and increases of SGOT to greater than five times baseline value were reported in 4% of patients receiving interferon beta-1b (compared to 1% on placebo), leading to dose-reduction or discontinuation of treatment in some patients [see Adverse Reactions (6.1)]. Monitor liver function tests [see Warnings and Precautions (5.10)].

5.2     Anaphylaxis And Other Allergic Reactions

Anaphylaxis has been reported as a rare complication of interferon beta-1b use. Other allergic reactions have included dyspnea, bronchospasm, tongue edema, skin rash, and urticaria [see Adverse Reactions (6.1)]. Discontinue EXTAVIA if anaphylaxis occurs.The removable rubber cap of the diluent (Sodium Chloride, 0.54% Solution) pre-filled syringe contains natural rubber latex, which may cause allergic reactions and should not be handled by latex-sensitive individuals. The safe use of EXTAVIA pre-filled syringe in latex-sensitive individuals has not been studied.

5.3     Depression And Suicide

Depression and suicide have been reported to occur with increased frequency in patients receiving interferon beta products, including interferon beta-1b. Advise patients to report any symptom of depression and/or suicidal ideation to their healthcare provider. If a patient develops depression, discontinuation of EXTAVIA therapy should be considered. In randomized controlled clinical trials, there were three suicides and eight suicide attempts among the 1532 patients on interferon beta-1b compared to one suicide and four suicide attempts among 965 patients on placebo.

5.4     Congestive Heart Failure

Monitor patients with preexisting congestive heart failure (CHF) for worsening of their cardiac condition during initiation of and continued treatment with EXTAVIA. While beta interferons do not have any known direct-acting cardiac toxicity, cases of CHF, cardiomyopathy, and cardiomyopathy with CHF have been reported in patients without known predisposition to these events, and without other known etiologies being established. In some cases, these events have been temporally related to the administration of interferon beta-1b. Recurrence upon rechallenge was observed in some patients. Consider discontinuation of EXTAVIA if worsening of CHF occurs with no other etiology.

5.5     Injection Site Necrosis And Reactions

Injection site necrosis (ISN) was reported in 4% of interferon beta-1b-treated patients in controlled clinical trials (compared to 0% on placebo) [see Adverse Reactions (6.1)]. Typically, ISN occurs within the first four months of therapy, although postmarketing reports have been received of ISN occurring over one year after initiation of therapy. The necrotic lesions are typically 3 cm or less in diameter, but larger areas have been reported. Generally the necrosis has extended only to subcutaneous fat, but has extended to the fascia overlying muscle. In some lesions where biopsy results are available, vasculitis has been reported. For some lesions, debridement, and/or skin grafting have been required. In most cases healing was associated with scarring. Whether to discontinue therapy following a single site of necrosis is dependent on the extent of necrosis. For patients who continue therapy with EXTAVIA after injection site necrosis has occurred, avoid administration of EXTAVIA into the affected area until it is fully healed. If multiple lesions occur, discontinue therapy until healing occurs.Periodically evaluate patient understanding and use of aseptic self-injection techniques and procedures, particularly if injection site necrosis has occurred.In controlled clinical trials, injection site reactions occurred in 78% of patients receiving interferon beta-1b with injection site necrosis in 4%. Injection site inflammation (42%), injection site pain (16%), injection site hypersensitivity (4%), injection site necrosis (4%), injection site mass (2%), injection site edema (2%) and nonspecific reactions were significantly associated with interferon beta-1b treatment. The incidence of injection site reactions tended to decrease over time. Approximately 69% of patients experienced injection site reactions during the first three months of treatment, compared to approximately 40% at the end of the studies.

5.6     Leukopenia

In controlled clinical trials, leukopenia was reported in 18% of patients receiving interferon beta-1b (compared to 6% on placebo), leading to a reduction of the dose of interferon beta-1b in some patients [see Adverse Reactions (6.1)]. Monitoring of complete blood and differential white blood cell counts is recommended. Patients with myelosuppression may require more intensive monitoring of complete blood cell counts, with differential and platelet counts.

5.7     Thrombotic Microangiopathy

Cases of thrombotic microangiopathy (TMA), including thrombotic thrombocytopenic purpura and hemolytic uremic syndrome, some fatal, have been reported with interferon beta products, including EXTAVIA. Cases have been reported several weeks to years after starting interferon beta products. Discontinue EXTAVIA if clinical symptoms and laboratory findings consistent with TMA occur, and manage as clinically indicated.

5.8     Flu-Like Symptom Complex

In controlled clinical trials, the rate of flu-like symptom complex for patients on interferon beta-1b was 57% [see Adverse Reactions (6.1)]. The incidence decreased over time, with 10% of patients reporting flu-like symptom complex at the end of the studies. The median duration of flu-like symptom complex in Study 1 was 7.5 days [see Clinical Studies (14)]. Analgesics and/or antipyretics on treatment days may help ameliorate flu-like symptoms associated with EXTAVIA use.

5.9     Seizures

Seizures have been temporally associated with the use of beta interferons in clinical trials and postmarketing safety surveillance. It is not known whether these events were related to a primary seizure disorder, the effects of multiple sclerosis alone, the use of beta interferons, other potential precipitants of seizures (e.g., fever), or to some combination of these.

5.10     Drug-Induced Lupus Erythematosus

Cases of drug-induced lupus erythematosus have been reported with some interferon beta products, including EXTAVIA. Signs and symptoms of drug-induced lupus reported in EXTAVIA-treated patients have included rash, serositis, polyarthritis, nephritis, and Raynaud’s phenomenon. Cases have occurred with positive serologic testing (including positive anti-nuclear and/or anti-double-stranded DNA antibody testing). If EXTAVIA-treated patients develop new signs and symptoms characteristic of this syndrome, EXTAVIA therapy should be stopped.

5.11     Monitoring For Laboratory Abnormalities

In addition to those laboratory tests normally required for monitoring patients with multiple sclerosis, complete blood and differential white blood cell counts, platelet counts and blood chemistries, including liver function tests, are recommended at regular intervals (one, three, and six months) following introduction of EXTAVIA therapy, and then periodically thereafter in the absence of clinical symptoms.

6     Adverse Reactions

  • The following serious adverse reactions are discussed in more details in other sections of labeling: •Hepatic Injury [see Warnings and Precautions (5.1)] •Anaphylaxis and Other Allergic Reactions [see Warnings and Precautions (5.2)] •Depression and Suicide [see Warnings and Precautions (5.3)] •Congestive Heart Failure [see Warnings and Precautions (5.4)] •Injection Site Necrosis and Reactions [see Warnings and Precautions (5.5)] •Leukopenia [see Warnings and Precautions (5.6)] •Thrombotic microangiopathy [see Warnings and Precautions (5.7)] •Flu-like Symptom Complex [see Warnings and Precautions (5.8)] •Seizures [see Warnings and Precautions (5.9)] •Drug Induced Lupus Erythematosus [see Warnings and Precautions (5.10)]

6.1     Clinical Trials Experience

Because clinical trials are conducted under widely varying conditions and over varying lengths of time, adverse reaction rates observed in the clinical trials of interferon beta-1b cannot be directly compared to rates in clinical trials of other drugs, and may not reflect the rates observed in practice. Among 1407 patients with MS treated with interferon beta-1b 0.25 mg every other day (including 1261 patients treated for greater than one year), the most commonly reported adverse reactions (at least 5% more frequent on interferon beta-1b than on placebo) were injection site reaction, lymphopenia, flu-like symptoms, myalgia leukopenia, neutropenia, increased liver enzymes, headache, hypertonia, pain, rash, insomnia, abdominal pain, and asthenia. The most frequently reported adverse reactions resulting in clinical intervention (for example, discontinuation of interferon beta-1b, adjustment in dosage, or the need for concomitant medication to treat an adverse reaction symptom) were depression, flu-like symptom complex, injection site reactions, leukopenia, increased liver enzymes, asthenia, hypertonia, and myasthenia.
Table 2 enumerates adverse reactions and laboratory abnormalities that occurred among patients treated with 0.25 mg of interferon beta-1b every other day by subcutaneous injection in the pooled placebo-controlled trials (Study 1-4) at an incidence that was at least 2% more than that observed in the placebo-treated patients [see Clinical Studies (14)].Table 2: Adverse Reactions and Laboratory Abnormalities in Patients with MS in Pooled Studies 1, 2, 3, and 4 Adverse ReactionPlacebo(N=965)Interferon beta-1b(N=1407)Blood and lymphatic system disordersLymphocytes count decreased (<1500/mm3)
66%86%Absolute neutrophil count decreased (<1500/mm3)
5%13%White blood cell count decreased (<3000/mm3)
4%13%Lymphadenopathy 3%6%Nervous system disordersHeadache43%50%Insomnia16%21%Incoordination15%17%Vascular disordersHypertension4%6%Respiratory, thoracic and mediastinal disorders Dyspnea3%6%Gastrointestinal disordersAbdominal pain11%16%Hepatobiliary disordersAlanine aminotransferase increased(SGPT > 5 times baseline)
4%12%Aspartate aminotransferase increased(SGOT > 5 times baseline)
1%4%Skin and subcutaneous tissue disordersRash15%21%Skin disorder8%10%Musculoskeletal and connective tissue disordersHypertonia33%40%Myalgia14%23%Renal and urinary disordersUrinary urgency8%11%Reproductive system and breast disordersMetrorrhagia7%9%Impotence6%8%General disorders and administration site conditionsInjection site reaction 126%78%Asthenia48%53%Flu-like symptoms (complex) 237%57%Pain35%42%Fever19%31%Chills9%21%Peripheral edema10%12%Chest pain6%9%Malaise3%6%Injection site necrosis0%4%1 "Injection site reaction" comprises all adverse reactions occurring at the injection site (except injection site necrosis), that is, the following terms: injection site reaction, injection site hemorrhage, injection site hypersensitivity, injection site inflammation, injection site mass, injection site pain, injection site edema and injection site atrophy.2 "Flu-like symptom (complex)" denotes flu syndrome and/or a combination of at least two adverse reactions from fever, chills, myalgia, malaise, sweating.In addition to the adverse reactions listed in Table 2, the following adverse reactions occurred more frequently on interferon beta-1b than on placebo, but with a difference smaller than 2%: alopecia, anxiety, arthralgia, constipation, diarrhea, dizziness, dyspepsia, dysmenorrhea, leg cramps, menorrhagia, myasthenia, nausea, nervousness, palpitations, peripheral vascular disorder, prostatic disorder, tachycardia, urinary frequency, vasodilatation, and weight increase.Laboratory AbnormalitiesIn the four clinical trials (Studies 1, 2, 3, and 4), leukopenia was reported in 18% and 6% of patients in interferon beta-1b- and placebo-treated groups, respectively. No patients were withdrawn or dose reduced for neutropenia in Study 1. Three percent (3%) of patients in Studies 2 and 3 experienced leukopenia and were dose-reduced. Other abnormalities included increase of SGPT to greater than five times baseline value (12%), and increase of SGOT to greater than five times baseline value (4%). In Study 1, two patients were dose reduced for increased hepatic enzymes; one continued on treatment and one was ultimately withdrawn. In Studies 2 and 3, 1.5% of interferon beta-1b patients were dose-reduced or interrupted treatment for increased hepatic enzymes. In Study 4, 1.7% of patients were withdrawn from treatment due to increased hepatic enzymes, two of them after a dose reduction. In Studies 1-4, nine (0.6%) patients were withdrawn from treatment with interferon beta-1b for any laboratory abnormality, including four (0.3%) patients following dose reduction.

6.2     Immunogenicity

As with all therapeutic proteins, there is a potential for immunogenicity. Serum samples were monitored for the development of antibodies to interferon beta-1b during Study 1. In patients receiving 0.25 mg every other day 56/124 (45%) were found to have serum neutralizing activity at one or more of the time points tested. In Study 4, neutralizing activity was measured every 6 months and at end of study. At individual visits after start of therapy, activity was observed in 17% up to 25% of the interferon beta-1b-treated patients. Such neutralizing activity was measured at least once in 75 (30%) out of 251 interferon beta-1b patients who provided samples during treatment phase; of these, 17 (23%) converted to negative status later in the study. Based on all the available evidence, the relationship between antibody formation and clinical safety or efficacy is not known.These data reflect the percentage of patients whose test results were considered positive for antibodies to interferon beta-1b using a biological neutralization assay that measures the ability of immune sera to inhibit the production of the interferon-inducible protein, MxA. Neutralization assays are highly dependent on the sensitivity and specificity of the assay. Additionally, the observed incidence of neutralizing activity in an assay may be influenced by several factors including sample handling, timing of sample collection, concomitant medications, and underlying disease. For these reasons, comparison of the incidence of antibodies to interferon beta-1b with the incidence of antibodies to other products may be misleading.Anaphylactic reactions have been reported with the use of interferon beta-1b [see Warnings and Precautions (5.2)].

6.3     Postmarketing Experience

The following adverse reactions have been identified during postapproval use of interferon beta-1b. Because these reactions are reported voluntarily from a population of uncertain size, it is not always possible to reliably estimate their frequency or establish a causal relationship to drug exposure.Blood and lymphatic system disorders: Anemia, ThrombocytopeniaEndocrine disorders: Hypothyroidism, Hyperthyroidism, Thyroid dysfunctionMetabolism and nutrition disorders: Triglyceride increased, Anorexia, Weight decrease, Weight increasePsychiatric disorders: Anxiety, Confusion, Emotional labilityNervous system disorders: Convulsion, Dizziness, Psychotic symptomsCardiac disorders: Cardiomyopathy, Palpitations, TachycardiaVascular disorders: VasodilatationRespiratory, thoracic and mediastinal disorders: BronchospasmGastrointestinal disorders: Diarrhea, Nausea, Pancreatitis, VomitingHepatobiliary disorders: Hepatitis, Gamma GT increasedSkin and subcutaneous tissue disorders: Alopecia, Pruritus, Skin discoloration, UrticariaMusculoskeletal and connective tissue disorders: Arthralgia; drug-induced lupus erythematosusReproductive system and breast disorder: MenorrhagiaGeneral disorders and administration site conditions: Fatal capillary leak syndrome*

*The administration of cytokines to patients with a preexisting monoclonal gammopathy has been associated with the development of this syndrome.

8.1     Pregnancy

Pregnancy Category C: There are no adequate and well-controlled studies in pregnant women; however, spontaneous abortions while on treatment were reported in four patients participating in the interferon beta-1b RRMS clinical trial. EXTAVIA should be used during pregnancy only if the potential benefit justifies the potential risk to the fetus. When interferon beta-1b (doses ranging from 0.028 to 0.42 mg/kg/day) was administered to pregnant rhesus monkeys throughout the period of organogenesis (gestation days 20 to 70), a dose-related abortifacient effect was observed. The low-effect dose is approximately 3 times the recommended human dose of 0.25 mg on a body surface area (mg/m2) basis. A no-effect dose for embryo-fetal developmental toxicity in rhesus monkeys was not established.

8.3     Nursing Mothers

It is not known whether interferon beta-1b is excreted in human milk. Because many drugs are excreted in human milk and because of the potential for serious adverse reactions in nursing infants from interferon beta-1b, a decision should be made to either discontinue nursing or discontinue the drug, taking into account the importance of drug to the mother.

8.4     Pediatric Use

Safety and efficacy in pediatric patients have not been established.

8.5     Geriatric Use

Clinical studies of interferon beta-1b did not include sufficient numbers of patients aged 65 and over to determine whether they respond differently than younger patients.

11     Description

EXTAVIA (interferon beta-lb) is a purified, sterile, lyophilized protein product produced by recombinant DNA techniques. Interferon beta-1b is manufactured by bacterial fermentation of a strain of Escherichia coli that bears a genetically engineered plasmid containing the gene for human interferon betaser17. The native gene was obtained from human fibroblasts and altered in a way that substitutes serine for the cysteine residue found at position 17. Interferon beta-1b has 165 amino acids and an approximate molecular weight of 18,500 daltons. It does not include the carbohydrate side chains found in the natural material. The specific activity of EXTAVIA is approximately 32 million international units (IU)/mg interferon beta-lb. Each vial contains 0.3 mg of interferon beta-lb. The unit measurement is derived by comparing the antiviral activity of the product to the World Health Organization (WHO) reference standard of recombinant human interferon beta. Mannitol, USP and Albumin (Human), USP (15 mg each/vial) are added as stabilizers.Lyophilized EXTAVIA is a sterile, white to off-white powder, for subcutaneous injection after reconstitution with the diluent supplied (Sodium Chloride, 0.54% Solution). Each vial contains Albumin (Human) USP (15 mg) and Mannitol, USP (15 mg).

12.1     Mechanism Of Action

The mechanism of action of EXTAVIA (interferon beta-1b) in patients with multiple sclerosis is unknown.

12.2     Pharmacodynamics

Interferons (IFNs) are a family of naturally occurring proteins, produced by eukaryotic cells in response to viral infection and other biologic agents. Three major types of interferons have been defined: type 1 (IFN-alpha, beta, epsilon, kappa and omega), type II (IFN–gamma) and type III (IFN-lambda). Interferon-beta is a member of the type I subset of interferons. The type I interferons have considerably overlapping but also distinct biologic activities. The bioactivities of all IFNs, including IFN-beta, are induced via their binding to specific receptors on the membranes of human cells. Differences in the bioactivities induced by the three major subtypes of IFNs likely reflect differences in the signal transduction pathways induced by signaling through their cognate receptors.Interferon beta-1b receptor binding induces the expression of proteins that are responsible for the pleiotropic bioactivities of interferon beta-1b. A number of these proteins (including neopterin, β2-microglobulin, MxA protein, and IL-10) have been measured in blood fractions from interferon beta-1b-treated patients and interferon beta-1b-treated healthy volunteers. Immunomodulatory effects of interferon beta-1b include the enhancement of suppressor T cell activity, reduction of pro-inflammatory cytokine production, down-regulation of antigen presentation, and inhibition of lymphocyte trafficking into the central nervous system. It is not known if these effects play an important role in the observed clinical activity of interferon beta-1b in multiple sclerosis (MS).

12.3     Pharmacokinetics

Because serum concentrations of interferon beta-1b are low or not detectable following subcutaneous administration of 0.25 mg or less of interferon beta-1b, pharmacokinetic information in patients with MS receiving the recommended dose of interferon beta-1b is not available. Following single and multiple daily subcutaneous administrations of 0.5 mg interferon beta-1b to healthy volunteers (N=12), serum interferon beta-1b concentrations were generally below 100 IU/mL. Peak serum interferon beta-1b concentrations occurred between one to eight hours, with a mean peak serum interferon concentration of 40 IU/mL. Bioavailability, based on a total dose of 0.5 mg interferon beta-1b given as two subcutaneous injections at different sites, was approximately 50%.After intravenous administration of interferon beta-1b (0.006 mg to 2 mg), similar pharmacokinetic profiles were obtained from healthy volunteers (N=12) and from patients with diseases other than MS (N=142). In patients receiving single intravenous doses up to 2 mg, increases in serum concentrations were dose proportional. Mean serum clearance values ranged from 9.4 mL/min•kg-1 to 28.9 mL/min•kg-1 and were independent of dose. Mean terminal elimination half-life values ranged from 8 minutes to 4.3 hours and mean steady-state volume of distribution values ranged from 0.25 L/kg to 2.88 L/kg. Three-times-a-week intravenous dosing for two weeks resulted in no accumulation of interferon beta-1b in sera of patients. Pharmacokinetic parameters after single and multiple intravenous doses of interferon beta-1b were comparable.Following every other day subcutaneous administration of 0.25 mg interferon beta-1b in healthy volunteers, biologic response marker levels (neopterin, β2-microglobulin, MxA protein, and the immunosuppressive cytokine, IL-10) increased significantly above baseline six-twelve hours after the first interferon beta-1b dose. Biologic response marker levels peaked between 40 and 124 hours and remained elevated above baseline throughout the seven-day (168-hour) study. The relationship between serum interferon beta-1b levels or induced biologic response marker levels and the clinical effects of interferon beta-1b in multiple sclerosis is unknown.Drug Interaction StudiesNo formal drug interaction studies have been conducted with interferon beta-1b.

13.1     Carcinogenesis, Mutagenesis, Impairment Of Fertility

CarcinogenesisInterferon beta-1b has not been tested for its carcinogenic potential in animals.MutagenesisInterferon beta-1b was not genotoxic in the in vitro Ames bacterial test or the in vitro chromosomal aberration assay in human peripheral blood lymphocytes. Interferon beta-1b treatment of mouse BALBc-3T3 cells did not result in increased transformation frequency in an in vitro model of tumor transformation.Impairment of FertilityAdministration of interferon beta-1b (doses of up to 0.33 mg/kg/day) to normally cycling female rhesus monkeys had no apparent adverse effects on either menstrual cycle duration or associated hormonal profiles (progesterone and estradiol) when administered over three consecutive menstrual cycles. The highest dose tested is approximately 30 times the recommended human dose of 0.25 mg on a body surface area (mg/m2) basis. The potential for other effects on fertility or reproductive performance was not evaluated.

14     Clinical Studies

The clinical effects of interferon beta-1b were studied in four randomized, multicenter, double-blind, placebo-controlled studies in patients with multiple sclerosis (Studies 1, 2, 3, and 4).Patients with Relapsing-Remitting Multiple SclerosisThe effectiveness of interferon beta-1b in relapsing-remitting MS (RRMS) was evaluated in a double blind, multiclinic, randomized, parallel, placebo controlled clinical study of two years duration (Study 1). The study enrolled MS patients, aged 18 to 50, who were ambulatory [Kurtzke Expanded Disability Status Scale (EDSS) of ≤5.5-score 5.5 is ambulatory for 100 meters, disability precludes full daily activities], exhibited a relapsing-remitting clinical course, met Poser’s criteria for clinically definite and/or laboratory supported definite MS and had experienced at least two exacerbations over two years preceding the trial without exacerbation in the preceding month. The EDSS score is a method of quantifying disability in patients with MS and ranges from 0 (normal neurologic exam) to 10 (death due to MS). Patients who had received prior immunosuppressant therapy were excluded.An exacerbation was defined as the appearance of a new clinical sign/symptom or the clinical worsening of a previous sign/symptom (one that had been stable for at least 30 days) that persisted for a minimum of 24 hours.Patients selected for study were randomized to treatment with either placebo (N=123), 0.05 mg of interferon beta-1b (N=125), or 0.25 mg of interferon beta-1b (N=124) self-administered subcutaneously every other day. Outcome based on the 372 randomized patients was evaluated after two years.Patients who required more than three 28-day courses of corticosteroids were removed from the study. Minor analgesics (acetaminophen, codeine), antidepressants, and oral baclofen were allowed ad libitum, but chronic nonsteroidal anti-inflammatory drug (NSAID) use was not allowed.The primary protocol-defined outcome measures were 1) frequency of exacerbations per patient and 2) proportion of exacerbation free patients. A number of secondary clinical and magnetic resonance imaging (MRI) measures were also employed. All patients underwent annual T2 MRI imaging and a subset of 52 patients at one site had MRIs performed every six weeks for assessment of new or expanding lesions. The study results are shown in Table 3.Table 3: Two-Year RRMS Study Results of Primary and Secondary Clinical Outcomes (Study 1)Efficacy Parameters Treatment GroupsStatistical Comparisons p-valuePrimary End Points Placebo(N=123)Interferon beta-1b0.05 mg(N=125)Interferon beta-1b0.25 mg(N=124)Placebovs0.05 mg0.05 mgvs0.25 mgPlacebovs0.25 mgAnnual exacerbation rate1.311.140.90.0050.1130.0001
Proportion of exacerbation-free patients116%18%25%0.6090.2880.094Exacerbation frequency per patient011234>520%32%20%15%15%21%22%31%28%15%7%16%29%39%17%14%9%8%0.1510.0770.001Secondary Endpoints2Median number of months to first on-study exacerbation5690.2990.0970.01Rate of moderate or severe exacerbations per year0.470. number of moderate or severe exacerbation days per patient4433200.2290.0640.001Mean change in EDSS score3 at endpoint0.210.21-0.070.9950.1080.144Mean change in Scripps score4 at endpoint-0.53-0.50.660.6410.0510.126Median duration in days per exacerbation363336ND5ND5ND5% change in mean MRI lesion area at endpoint21.4%9.8%-0.9%0.0150.0190.00011 14 exacerbation free patients (0 from placebo, six from 0.05 mg, and eight from 0.25 mg) dropped out of the study before completing six months of therapy. These patients are excluded from this analysis.2 Sequelae and Functional Neurologic Status, both required by protocol, were not analyzed individually but are included as a function of the EDSS.3 EDSS scores range from 1-10, with higher scores reflecting greater disability.4 Scripps neurologic rating scores range from 0-100, with smaller scores reflecting greater disability.5 ND=Not done.
Of the 372 RRMS patients randomized, 72 (19%) failed to complete two full years on their assigned treatments. Over the two-year period in Study 1, there were 25 MS-related hospitalizations in the 0.25 mg interferon beta-1b-treated group compared to 48 hospitalizations in the placebo group. In comparison, non-MS hospitalizations were evenly distributed among the groups, with 16 in the 0.25 mg interferon beta-1b group and 15 in the placebo group. The average number of days of MS-related steroid use was 41 days in the 0.25 mg interferon beta-1b group and 55 days in the placebo group (p=0.004).MRI data were also analyzed for patients in this study. A frequency distribution of the observed percent changes in MRI area at the end of two years was obtained by grouping the percentages in successive intervals of equal width. Figure 1 displays a histogram of the proportions of patients, which fell into each of these intervals. The median percent change in MRI area for the 0.25 mg group was -1.1%, which was significantly smaller than the 16.5% observed for the placebo group (p=0.0001).Figure 1: Distribution of Change in MRI Area in Patients with RRMS in Study 1In an evaluation of frequent MRI scans (every six weeks) on 52 patients at one site in Study 1, the percent of scans with new or expanding lesions was 29% in the placebo group and 6% in the 0.25 mg treatment group (p=0.006).The exact relationship between MRI findings and clinical status of patients is unknown. Changes in lesion area often do not correlate with changes in disability progression. The prognostic significance of the MRI findings in this study has not been evaluated.Patients with Secondary Progressive Multiple Sclerosis Studies 2 and 3 were multicenter, randomized, double-blind, placebo-controlled trials conducted to assess the effect of interferon beta-1b in patients with secondary progressive MS (SPMS). Study 2 was conducted in Europe and Study 3 was conducted in North America. Both studies enrolled patients with clinically definite or laboratory-supported MS in the secondary progressive phase, and who had evidence of disability progression (both Study 2 and 3) or two relapses (Study 2 only) within the previous two years. Baseline Kurtzke expanded disability status scale (EDSS) scores ranged from 3.0 to 6.5. Patients in Study 2 were randomized to receive interferon beta-1b 0.25 mg (N=360) or placebo (N=358). Patients in Study 3 were randomized to interferon beta-1b 0.25 mg (N=317), interferon beta-1b 0.16 mg/m2 of body surface area (N=314, mean assigned dose 0.3 mg), or placebo (N=308). Test agents were administered subcutaneously, every other day for three years.The primary outcome measure was progression of disability, defined as a 1.0 point increase in the EDSS score, or a 0.5 point increase for patients with baseline EDSS ≥ 6.0. In Study 2, time to progression in EDSS was longer in the interferon beta-1b treatment group (p=0.005), with estimated annualized rates of progression of 16% and 19% in the interferon beta-1b and placebo groups, respectively. In Study 3, the rates of progression did not differ significantly between treatment groups, with estimated annualized rates of progression of 12%, 14%, and 12% in the interferon beta-1b fixed dose, surface area-adjusted dose, and placebo groups, respectively.Multiple analyses, including covariate and subset analyses based on sex, age, disease duration, clinical disease activity prior to study enrollment, MRI measures at baseline and early changes in MRI following treatment were evaluated in order to interpret the discordant study results. No demographic or disease-related factors enabled identification of a patient subset where interferon beta-1b treatment was predictably associated with delayed progression of disability.In Studies 2 and 3, like Study 1, a statistically significant decrease in the incidence of relapses associated with interferon beta-1b treatment was demonstrated. In Study 2, the mean annual relapse rates were 0.42 and 0.63 in the interferon beta-1b and placebo groups, respectively (p<0.001). In Study 3, the mean annual relapse rates were 0.16, 0.20, and 0.28, for the fixed dose, surface area-adjusted dose, and placebo groups, respectively (p<0.02).MRI endpoints in both Study 2 and Study 3 showed smaller increases in T2 MRI lesion area and decreased number of active MRI lesions in patients in the interferon beta-1b groups compared to the placebo group. The exact relationship between MRI findings and the clinical status of patients is unknown. Changes in MRI findings often do not correlate with changes in disability progression. The prognostic significance of the MRI findings in these studies is not known.Patients with an Isolated Demyelinating Event and Typical MS Lesions on Brain MRI In Study 4, 468 patients who had recently (within 60 days) experienced an isolated demyelinating event, and who had lesions typical of multiple sclerosis on brain MRI were randomized to receive either 0.25 mg interferon beta-1b (N=292) or placebo (N=176) subcutaneously every other day (ratio 5:3). The primary outcome measure was time to development of a second exacerbation with involvement of at least two distinct anatomical regions. Secondary outcomes were brain MRI measures, including the cumulative number of newly active lesions, and the absolute change in T2 lesion volume. Patients were followed for up to two years or until they fulfilled the primary endpoint. Eight percent of subjects on interferon beta-1b and 6% of subjects on placebo withdrew from the study for a reason other than the development of a second exacerbation. Time to development of a second exacerbation was significantly delayed in patients treated with interferon beta-1b compared to patients treated with placebo (p<0.0001). The Kaplan-Meier estimates of the percentage of patients developing an exacerbation within 24 months were 45% in the placebo group and 28% of the interferon beta-1b group (Figure 2). The risk for developing a second exacerbation in the interferon beta-1b group was 53% of the risk in the placebo group (Hazard ratio= 0.53; 95% confidence interval 0.39 to 0.73).Figure 2: Onset of Second Exacerbation by Time in Patients with Isolated Demyelinating Event with Typical MS Lesions on Brain MRI in Study 4**Kaplan-Meier Methodology In Study 4, patients treated with interferon beta-1b demonstrated a lower number of newly active lesions during the course of the study. A significant difference between interferon beta-1b and placebo was not seen in the absolute change in T2 lesion volume during the course of the study.Safety and efficacy of treatment with interferon beta-1b beyond three years are not known.

16.1 How Supplied

EXTAVIA is supplied as a lyophilized powder in a clear glass, single-use vial (3 mL capacity). Each carton contains 15 blister units: NDC 0078-0569-12. Each blister unit contains:A single-use vial containing 0.3 mg EXTAVIA (interferon beta-1b)A pre-filled single-use syringe containing 1.2 mL diluent (Sodium Chloride, 0.54% solution). The rubber cap of the pre-filled syringe contains natural rubber latex.A vial adapter with a 27-gauge needle attached2 alcohol prep pads

16.2 Stability And Storage

EXTAVIA and the diluent are for single-use only. Discard unused portions. The reconstituted product contains no preservative. Store EXTAVIA vials at room temperature 68°F to 77°F (20°C to 25°C). Excursions of 59°F to 86°F (15°C to 30°C) are permitted for up to 3 months. After reconstitution, if not used immediately, refrigerate the reconstituted solution and use within three hours. Do not freeze.

17     Patient Counseling Information

Advise the patient to read the FDA-approved patient labeling (Medication Guide and Instructions for Use).Instruction on Self-Injection Technique and ProceduresProvide appropriate instruction for reconstitution of EXTAVIA and methods of self-injection, including careful review of the EXTAVIA Medication Guide. Instruct patients in the use of aseptic technique when administering EXTAVIA.Tell patients not to re-use needles or syringes and instruct patients on safe disposal procedures. Advise patients of the importance of rotating areas of injection with each dose, to minimize the likelihood of severe injection site reactions, including necrosis or localized infection [see Medication Guide]. Hepatic InjuryAdvise patients that severe hepatic injury, including hepatic failure, has been reported during the use of EXTAVIA.Inform patients of symptoms of hepatic dysfunction, and instruct patients to report them immediately to their healthcare provider [see Warnings and Precautions (5.1)].Anaphylaxis and Other Allergic Reactions Advise patients of the symptoms of allergic reactions and anaphylaxis, and instruct patients to seek immediate medical attention if these symptoms occur. Inform latex-sensitive patients that the removable rubber cap of the diluent pre-filled syringe contains natural rubber latex [see Warnings and Precautions (5.2)].Depression and SuicideAdvise patients that depression and suicidal ideation have been reported during the use of EXTAVIA. Inform patients of the symptoms of depression or suicidal ideation, and instruct patients to report them immediately to their healthcare provider [see Warnings and Precautions (5.3)].Congestive Heart FailureAdvise patients that worsening of preexisting congestive heart failure have been reported in patients using EXTAVIA.Advise patients of symptoms of worsening cardiac condition, and instruct patients to report them immediately to their healthcare provider [see Warnings and Precautions (5.4)].Injection Site Necrosis and ReactionsAdvise patients that injection site reactions occur in most patients treated with EXTAVIA, and that injection site necrosis may occur at one or multiple sites. Instruct patients to promptly report any break in the skin, which may be associated with blue-black discoloration, swelling, or drainage of fluid from the injection site, prior to continuing their EXTAVIA therapy [see Warnings and Precautions (5.5)].Flu-like Symptom ComplexInform patients that flu-like symptoms are common following initiation of therapy with EXTAVIA, and that concurrent use of analgesics and/or antipyretics on treatment days may help ameliorate flu-like symptoms associated with EXTAVIA use [see Warnings and Precautions (5.8) and Dosage and Administration (2.4)].SeizuresInstruct patients to report seizures immediately to their healthcare provider [see Warnings and Precautions (5.9)].Drug Induced Lupus ErythematosusAdvise patients that drug-induced lupus erythematosus has been reported during the use of EXTAVIA. Inform patients of the symptoms of rash, redness of the skin on the face, joint pain, fever and weakness, and instruct patients to report them immediately to their healthcare provider [see Warnings and Precautions (5.10)].PregnancyAdvise patients that EXTAVIA should not be used during pregnancy unless the potential benefit justifies the potential risk to the fetus [see Use in Special Population (8.1)]. Therefore, inform patients that if a pregnancy is considered, or does occur, the risks and benefits of continuing EXTAVIA should be discussed with their healthcare provider.Distributed by:Novartis Pharmaceuticals CorporationEast Hanover, New Jersey 07936© NovartisT2016-35May 2016

Spl Medguide

  • Medication GuideEXTAVIA(ex tā vee uh)interferon beta-1b (in-ter-feer-on beta-one-be)Read this Medication Guide before you start taking EXTAVIA and each time you get a refill. There may be new information. This information does not take the place of talking with your healthcare provider about your medical condition or your treatment. What is the most important information I should know about EXTAVIA?EXTAVIA can cause serious side effects, including: •liver problems including liver failure. Symptoms of liver problems may include: •yellowing of your eyes •itchy skin •feeling very tired •flu-like symptoms •nausea or vomiting •bruising easily or bleeding problemsYour healthcare provider will do blood tests to check for these problems while you take EXTAVIA. •serious allergic reactions. Serious allergic reactions can happen quickly and may happen after your first dose of EXTAVIA or after you have taken EXTAVIA many times. Symptoms may include: •difficulty breathing or swallowing •swelling of the mouth or tongue •rash, itching, or skin bumps •depression or suicidal thoughts. Call your healthcare provider right away if you have any of the following symptoms, especially if they are new, worse, or worry you: •thoughts about suicide or dying •new or worse depression •new or worse anxiety •trouble sleeping (insomnia) •acting aggressive, being angry, or violent •acting on dangerous impulses •hallucinations •other unusual changes in behavior or moodWhat is EXTAVIA? EXTAVIA is a prescription medicine used to reduce the number of relapses in people with relapsing forms of multiple sclerosis (MS). This includes people who have had their first symptoms of multiple sclerosis and have an MRI consistent with multiple sclerosis. EXTAVIA is similar to certain interferon proteins that are produced in the body. It will not cure your MS but may decrease the number of flare-ups of the disease. It is not known if EXTAVIA is safe and effective in children. Who should not take EXTAVIA?Do not take EXTAVIA if you are allergic to interferon beta-1b, to another interferon beta, to human albumin, or mannitol. See the end of this leaflet for a complete list of ingredients in EXTAVIA. What should I tell my healthcare provider before taking EXTAVIA?Before you take EXTAVIA, tell your healthcare provider if you: •have or have had depression (sinking feeling or sadness), anxiety (feeling uneasy, nervous, or fearful for no reason) or trouble sleeping •have or have had liver problems •have or have had blood problems such as bleeding or bruising easily, low red blood cells (anemia) or low white blood cells •have or have had seizures •have or have had heart problems •have or have had an allergic reaction to rubber or latex. The rubber cap of the diluent pre-filled syringe contains natural rubber latex. •are pregnant or plan to become pregnant. EXTAVIA can harm your unborn baby. EXTAVIA may cause you to lose your baby (miscarry). If you become pregnant while taking EXTAVIA call your healthcare provider right away. You and your healthcare provider should decide if you should continue to take EXTAVIA. •are breastfeeding or plan to breastfeed. It is not known if EXTAVIA passes into your breast milk. You and your healthcare provider should decide if you will take EXTAVIA or breastfeed. You should not do both. Tell your healthcare provider about all the medicines you take, including prescription and nonprescription medicines, vitamins, and herbal supplements. Know the medicines you take. Keep a list of them to show your healthcare provider and pharmacist when you get a new medicine. How should I take EXTAVIA? •See the Instructions for Use at the end of this Medication Guide for complete information on how to use EXTAVIA. •EXTAVIA is given by injection under your skin (subcutaneous injection) every other day. •Take EXTAVIA exactly as your healthcare provider tells you to take it. •If your healthcare provider feels that you or someone else may give you the injections then you or the other person should be trained by your healthcare provider in how to give an injection. •Do not try to give yourself or have another person give you injections until you or both of you understand and are comfortable with how to prepare your dose and give the injection. •You may be started on a lower dose when you first start taking EXTAVIA. Your healthcare provider will tell you what dose of EXTAVIA to use. •Your healthcare provider may change your dose of EXTAVIA. You should not change your dose without talking to your healthcare provider. •If you miss a dose, you should take your next dose as soon as you remember or are able to take it. Your next injection should be taken about 48 hours (2 days) after that dose. Do not take EXTAVIA on 2 consecutive days. If you accidentally take more than your prescribed dose, or take it on 2 consecutive days, call your healthcare provider right away. •Always use a new, unopened vial of EXTAVIA and pre-filled diluent syringe for each injection. Throw away any unused medicine. Do not re-use any vials, syringes, or needles. •It is important for you to change your injection site each time you inject EXTAVIA. This will lessen the chance of you having a serious skin reaction at the site where you inject EXTAVIA. Avoid injecting EXTAVIA into an area of skin that is sore, reddened, infected or has other problems.What are the possible side effects of EXTAVIA?EXTAVIA may cause serious side effects. Call your healthcare provider right away if you have any of the serious side effects of EXTAVIA including: •See “What is the most important information I should know about EXTAVIA?” •heart problems. EXTAVIA may worsen heart problems including congestive heart failure. Symptoms of heart problems may include: •swollen ankles •shortness of breath •decreased ability to exercise •fast heartbeat •tightness in chest •increased need to urinate at night •not being able to lay flat in bed •injection site problems. Serious skin reactions can happen in some people including areas of severe damage to skin and the tissue below the skin (necrosis). These reactions can happen anywhere you inject EXTAVIA. Symptoms of injection site problems may include: •swelling, redness, or pain at the injection site •fluid drainage from the injection site •breaks in your skin or blue-black skin discoloration •flu-like symptoms. EXTAVIA can cause flu-like symptoms including: •fever •chills •tiredness •sweating •muscle aches when you first start to use it  These symptoms may decrease over time. Taking medicines for fever and pain relief on the days you are using EXTAVIA may help decrease these symptoms. •seizures. Some people have had seizures while taking EXTAVIA, including people who have never had seizures before. It is not known if the seizures were related to their MS, to EXTAVIA, or to a combination of both. If you have a seizure after taking EXTAVIA call your healthcare provider right away.  The most common side effects of EXTAVIA include: •low white blood cell count •increases in your liver enzymes •headache •increases in your muscle tension •pain •rash •problems sleeping •stomach pain •weakness  Tell your healthcare provider if you have any side effect that bothers you or that does not go away. These are not all the possible side effects of EXTAVIA. For more information, ask your healthcare provider or pharmacist. Call your doctor for medical advice about side effects. You may report side effects to FDA at 1-800-FDA-1088. How should I store EXTAVIA? •Before mixing, store EXTAVIA at room temperature between 68°F to 77°F (20°C to 25°C). •Before mixing, EXTAVIA may be stored for up to 3 months between 59°F to 86°F (15°C to 30°C). •After mixing, you can refrigerate EXTAVIA for up to 3 hours before using. Your EXTAVIA must be used within 3 hours of mixing even if refrigerated. •Do not freeze. Keep EXTAVIA and all medicines out of the reach of children.General information about the safe and effective use of EXTAVIA.Medicines are sometimes prescribed for purposes other than those listed in a Medication Guide. Do not use EXTAVIA for a condition for which it was not prescribed. Do not give EXTAVIA to other people, even if they have the same symptoms that you have. It may harm them.This Medication Guide summarizes the most important information about EXTAVIA. If you would like more information, talk with your healthcare provider. You can ask your pharmacist or healthcare provider for information about EXTAVIA that is written for health professionals.For more information, go to www.EXTAVIA.com or call the EXTAVIA toll-free medical information line at 1-888-669-6682.What are the ingredients in EXTAVIA?Active ingredient: interferon beta-1bInactive ingredients: albumin (human), mannitolDiluent contains sodium chloride solution.Manufactured by:Bayer HealthCare Pharmaceuticals Inc.Whippany, NJ 07981Distributed by:Novartis Pharmaceuticals CorporationEast Hanover, NJ 07936ForNovartis Pharmaceuticals CorporationEast Hanover, NJ 07936U.S. License No. 1244This Medication Guide has been approved by the U.S. Food and Drug Administration© NovartisT2016-36May 2016

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