NDC 51662-1423 Nitroglycerin Lingual

Nitroglycerin Lingual

NDC Product Code 51662-1423

NDC CODE: 51662-1423

Proprietary Name: Nitroglycerin Lingual What is the Proprietary Name?
The proprietary name also known as the trade name is the name of the product chosen by the medication labeler for marketing purposes.

Non-Proprietary Name: Nitroglycerin Lingual What is the Non-Proprietary Name?
The non-proprietary name is sometimes called the generic name. The generic name usually includes the active ingredient(s) of the product.

Drug Use Information

Drug Use Information
The drug use information is a summary and does NOT have all possible information about this product. This information does not assure that this product is safe, effective, or appropriate. This information is not individual medical advice and does not substitute for the advice of a health care professional. Always ask a health care professional for complete information about this product and your specific health needs.

  • This medication is used to relieve chest pain (angina) in people that have a certain heart condition (coronary artery disease). It may also be used before physical activities (such as exercise, sexual activity) to help prevent chest pain. Nitroglycerin belongs to a class of drugs known as nitrates. Angina occurs when the heart muscle is not getting enough blood. This drug works by relaxing and widening blood vessels so blood can flow more easily to the heart.

NDC Code Structure

  • 51662 - Hf Acquisition Co Llc, Dba Healthfirst

NDC 51662-1423-1

Package Description: 60 SPRAY in 1 BOTTLE

NDC Product Information

Nitroglycerin Lingual with NDC 51662-1423 is a a human prescription drug product labeled by Hf Acquisition Co Llc, Dba Healthfirst. The generic name of Nitroglycerin Lingual is nitroglycerin lingual. The product's dosage form is spray and is administered via oral form.

Labeler Name: Hf Acquisition Co Llc, Dba Healthfirst

Dosage Form: Spray - A liquid minutely divided as by a jet of air or steam.

Product Type: Human Prescription Drug What kind of product is this?
Indicates the type of product, such as Human Prescription Drug or Human Over the Counter Drug. This data element matches the “Document Type” field of the Structured Product Listing.

Nitroglycerin Lingual Active Ingredient(s)

What is the Active Ingredient(s) List?
This is the active ingredient list. Each ingredient name is the preferred term of the UNII code submitted.

  • NITROGLYCERIN 400 ug/1

Inactive Ingredient(s)

About the Inactive Ingredient(s)
The inactive ingredients are all the component of a medicinal product OTHER than the active ingredient(s). The acronym "UNII" stands for “Unique Ingredient Identifier” and is used to identify each inactive ingredient present in a product.

  • ALCOHOL (UNII: 3K9958V90M)
  • MEDIUM-CHAIN TRIGLYCERIDES (UNII: C9H2L21V7U)
  • PEPPERMINT (UNII: V95R5KMY2B)

Administration Route(s)

What are the Administration Route(s)?
The translation of the route code submitted by the firm, indicating route of administration.

  • Oral - Administration to or by way of the mouth.
  • Oral - Administration to or by way of the mouth.

Pharmacological Class(es)

What is a Pharmacological Class?
These are the reported pharmacological class categories corresponding to the SubstanceNames listed above.

  • Nitrate Vasodilator - [EPC] (Established Pharmacologic Class)
  • Nitrates - [CS]
  • Vasodilation - [PE] (Physiologic Effect)

Product Labeler Information

What is the Labeler Name?
Name of Company corresponding to the labeler code segment of the Product NDC.

Labeler Name: Hf Acquisition Co Llc, Dba Healthfirst
Labeler Code: 51662
FDA Application Number: ANDA091496 What is the FDA Application Number?
This corresponds to the NDA, ANDA, or BLA number reported by the labeler for products which have the corresponding Marketing Category designated. If the designated Marketing Category is OTC Monograph Final or OTC Monograph Not Final, then the Application number will be the CFR citation corresponding to the appropriate Monograph (e.g. “part 341”). For unapproved drugs, this field will be null.

Marketing Category: ANDA - A product marketed under an approved Abbreviated New Drug Application. What is the Marketing Category?
Product types are broken down into several potential Marketing Categories, such as NDA/ANDA/BLA, OTC Monograph, or Unapproved Drug. One and only one Marketing Category may be chosen for a product, not all marketing categories are available to all product types. Currently, only final marketed product categories are included. The complete list of codes and translations can be found at www.fda.gov/edrls under Structured Product Labeling Resources.

Start Marketing Date: 10-09-2019 What is the Start Marketing Date?
This is the date that the labeler indicates was the start of its marketing of the drug product.

Listing Expiration Date: 12-31-2021 What is the Listing Expiration Date?
This is the date when the listing record will expire if not updated or certified by the product labeler.

Exclude Flag: N What is the NDC Exclude Flag?
This field indicates whether the product has been removed/excluded from the NDC Directory for failure to respond to FDA’s requests for correction to deficient or non-compliant submissions. Values = ‘Y’ or ‘N’.

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Information for Patients

Nitroglycerin Spray

Nitroglycerin Spray is pronounced as (nye troe gli' ser in)

Why is nitroglycerin spray medication prescribed?
Nitroglycerin spray is used to treat episodes of angina (chest pain) in people who have coronary artery disease (narrowing of the blood vessels that supply blood to the h...
[Read More]

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Nitroglycerin Lingual 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

Highlights Of Prescribing Information

These highlights do not include all the information needed to use NITROGLYCERIN LINGUAL SPRAY safely and effectively.

See full prescribing information for NITROGLYCERIN LINGUAL SPRAY.

Nitroglycerin Lingual Spray

Initial U.S. Approval: 1997
INDICATIONS AND USAGENitroglycerin Lingual Spray is a nitrate vasodilator indicated for acute relief of an attack or prophylaxis of angina pectoris due to coronary artery disease. (
1)
DOSAGE AND ADMINISTRATION•

At the onset of an attack, administer onto or under the tongue. Repeat every 5 minutes as needed (2.1).



Do up to three metered sprays within a 15-minute period. If chest pain persists, advise prompt medical attention (2.1).



May be used prophylactically 5 to 10 minutes prior to engaging in activities that might precipitate an acute attack (2.1).
DOSAGE FORMS AND STRENGTHSLingual spray, 400 mcg per spray, available in 60 or 200 metered sprays per container. (
3)
CONTRAINDICATIONS•

Use of phosphodiesterase type 5 (PDE5) inhibitors, such as avanafil, sildenafil, tadalafil, or vardenafil, or soluble guanylate cyclase (sGC) stimulator (riociguat). (4.1)



Severe anemia. (4.2)



Increased intracranial pressure. (4.3)



History of hypersensitivity to Nitroglycerin Lingual Spray or to other nitrates or nitrites or any excipient. (4.4)
WARNINGS AND PRECAUTIONSTolerance: Excessive use may lead to tolerance. (5)Hypotension: Severe hypotension may occur. (5)ADVERSE REACTIONSMost common adverse reactions occurring at a frequency greater than 2% are headache, dizziness and paresthesia (6).To report SUSPECTED ADVERSE REACTIONS, contact Perrigo at 1-866-634-9120 or FDA at 1-800-FDA-1088 or www.fda.gov/medwatch.DRUG INTERACTIONS•

Antihypertensives: Possible additive hypotensive effects. (7.2)



Ergotamine: increased bioavailability of ergotamine. Avoid concomitant use (7.4)
See 17 for PATIENT COUNSELING INFORMATION and PATIENT COUNSELING INFORMATION.Revised: 10/2018

Full Prescribing Information: Contents*

1 INDICATIONS AND USAGE
2 DOSAGE AND ADMINISTRATION

2.1 Recommended dosage

2.2 Priming

2.3 Administration
3 DOSAGE FORMS AND STRENGTHS
4 CONTRAINDICATIONS

4.1 PDE-5-Inhibitors and sGC-Stimulators

4.2 Severe Anemia

4.3 Increased Intracranial Pressure

4.4 Hypersensitivity

4.5 Circulatory Failure and Shock
5 WARNINGS AND PRECAUTIONS

5.1 Tolerance

5.2 Hypotension

5.3 Hypertrophic Obstructive Cardiomyopathy

5.4 Headache
6 ADVERSE REACTIONS

6.1 Clinical Trials Experience

6.2 Postmarketing Experience
7 DRUG INTERACTIONS

7.1 PDE-5-inhibitors and sGC-Stimulators

7.2 Antihypertensives

7.3 Ergotamine
8 USE IN SPECIFIC POPULATIONS

8.1 Pregnancy

8.3 Nursing Mothers

8.4 Pediatric Use

8.5 Geriatric Use
10 OVERDOSAGE

10.1 Signs and symptoms, methemoglobinemia

10.2 Treatment of overdosage
11 DESCRIPTION
12 CLINICAL PHARMACOLOGY

12.1 Mechanism of action

12.2 Pharmacodynamics

12.3 Pharmacokinetics
13 NONCLINICAL TOXICOLOGY

13.1 Carcinogenesis, Mutagenesis, Impairment of Fertility
14 CLINICAL STUDIES
16 HOW SUPPLIED/STORAGE AND HANDLING
17 PATIENT COUNSELING INFORMATION
*

Sections or subsections omitted from the full prescribing information are not listed.

1 Indications & Usage

Nitroglycerin Lingual Spray is indicated for acute relief of an attack or prophylaxis of angina pectoris due to coronary artery disease.

2 Dosage & Administration

2.1 Recommended dosageInstruct the patient to administer one or two metered sprays (400 mcg of nitroglycerin per spray) at the onset of an attack onto or under the tongue. A spray may be repeated approximately every five minutes as needed. No more than three metered sprays are recommended within a 15-minute period. If the chest pain persists after a total of three sprays, advise prompt medical attention. Nitroglycerin Lingual Spray may be used prophylactically 5 to 10 minutes prior to engaging in activities that might precipitate an acute attack.2.2 PrimingThe pump must be primed prior to the first use. Each metered spray of Nitroglycerin Lingual Spray delivers 48 mg of solution containing 400 mcg of nitroglycerin after an initial priming of five sprays. It will remain adequately primed for 6 weeks. If the product is not used within 6 weeks it can be adequately re-primed with one spray. If the product is not used within 3 months it can be adequately re-primed with up to five sprays. There are 60 or 200 metered sprays per bottle. The total number of available doses is dependent, however, on the number of sprays per use (1 or 2 sprays), and the frequency of priming.2.3 AdministrationInstruct patients that during administration, the patient should rest, ideally in the sitting position. Hold the container vertically with the valve head uppermost and the spray orifice as close to the mouth as possible. Spray the dose preferably onto or under the tongue by pressing the grooved-button firmly and the mouth closed immediately after each dose. THE SPRAY SHOULD NOT BE INHALED. The medication should not be expectorated or the mouth rinsed for 5 to 10 minutes following administration. Instruct patients to familiarize themselves with the position of the spray orifice, which can be identified by the finger rest on top of the valve, in order to facilitate orientation for administration at night [see Patient Information (17)].The amount of liquid remaining in the container should be checked periodically. The transparent container can be used for continuous monitoring of the consumption. With the container upright and level, check to be sure the end of the center tube extends below the level of the liquid. Once fluid falls below the level of the center tube, remaining sprays will not deliver intended dose.

3 Dosage Forms & Strengths

Lingual spray, 400 mcg per spray available in either 60 or 200 metered sprays per container.

4 Contraindications

4.1 PDE-5-Inhibitors and sGC-StimulatorsDo not use Nitroglycerin Lingual Spray in patients who are taking PDE-5 inhibitors, such as avanafil, sildenafil, tadalafil, or vardenafil. Concomitant use can cause severe hypotension, syncope, or myocardial ischemia [see Drug Interactions (7.1)].Do not use Nitroglycerin Lingual Spray in patients who are taking the soluble guanylate cyclase (sGC) stimulator riociguat. Concomitant use can cause hypotension.4.2 Severe AnemiaNitroglycerin Lingual Spray is contraindicated in patients with severe anemia (large doses of nitroglycerin may cause oxidation of hemoglobin to methemoglobin and could exacerbate anemia).4.3 Increased Intracranial PressureNitroglycerin Lingual Spray may precipitate or aggravate increased intracranial pressure and thus should not be used in patients with possible increased intracranial pressure (e. g. cerebral hemorrhage or traumatic brain injury).4.4 HypersensitivityNitroglycerin Lingual Spray is contraindicated in patients who are allergic to nitroglycerin, other nitrates or nitrites or any excipient.4.5 Circulatory Failure and ShockNitroglycerin Lingual Spray is contraindicated in patients with acute circulatory failure or shock.

5 Warnings And Precautions

5.1 ToleranceExcessive use may lead to the development of tolerance. Only the smallest number of doses required for effective relief of the acute angina attack should be used [see Dosage and Administration (2.1)].5.2 HypotensionSevere hypotension, particularly with upright posture, may occur even with small doses of nitroglycerin particularly in patients with constrictive pericarditis, aortic or mitral stenosis, patients who may be volume-depleted, or are already hypotensive. Hypotension induced by nitroglycerin may be accompanied by paradoxical bradycardia and increased angina pectoris. Symptoms of severe hypotension (nausea, vomiting, weakness, pallor, perspiration and collapse/syncope) may occur even with therapeutic doses.5.3 Hypertrophic Obstructive CardiomyopathyNitrate therapy may aggravate the angina caused by hypertrophic obstructive cardiomyopathy.5.4 HeadacheNitroglycerin produces dose-related headaches, especially at the start of nitroglycerin therapy, which may be severe and persistent but usually subside with continued use.

6 Adverse Reactions

6.1 Clinical Trials ExperienceBecause clinical trials are conducted under widely varying conditions, adverse reaction rates observed in the clinical trials of a drug cannot be directly compared to rates in the clinical trials of another drug and may not reflect the rates observed in clinical practice.Adverse reactions occurring at a frequency greater than 2% and greater than placebo included: headache, dizziness, and paresthesia.6.2 Postmarketing ExperienceThe following adverse reactions have been identified during postapproval use of nitroglycerin lingual spray and other nitroglycerin drugs. Because these reactions are reported voluntarily from a population of uncertain size, it is not always possible to estimate their frequency reliably or establish a causal relationship to drug exposure.Neurologic: weakness, drowsinessDermatologic: cutaneous vasodilation, flushing, drug rash, exfoliative dermatitisGastrointestinal: nausea, vomitingRespiratory: transient hypoxemiaCardiovascular: tachycardia

7 Drug Interactions

7.1 PDE-5-inhibitors and sGC-StimulatorsNitroglycerin Lingual Spray is contraindicated in patients who are using a selective inhibitor of cyclic guanosine monophosphate (cGMP)-specific phosphodiesterase type 5 (PDE5). PDE5 inhibitors such as avanafil, sildenafil, vardenafil, and tadalafil have been shown to potentiate the hypotensive effects of organic nitrates.Do not use Nitroglycerin Lingual Spray in patients who are taking the soluble guanylate cyclase (sGC) stimulator riociguat. Concomitant use can cause hypotension.The time course and dose dependence of these interactions have not been studied, and use within a few days of one another cannot be recommended. Appropriate supportive care for the severe hypotension has not been studied, but it seems reasonable to treat this as a nitrate overdose, with elevation of the extremities and with central volume expansion.7.2 AntihypertensivesPatients receiving antihypertensive drugs, beta-adrenergic blockers, and nitrates should be observed for possible additive hypotensive effects. Marked orthostatic hypotension has been reported when calcium channel blockers and organic nitrates were used concomitantly.Beta-adrenergic blockers blunt the reflex tachycardia produced by nitroglycerin without preventing its hypotensive effects. If beta-blockers are used with nitroglycerin in patients with angina pectoris, additional hypotensive effects may occur.7.3 ErgotamineOral administration of nitroglycerin markedly decreases the first-pass metabolism of dihydroergotamine and subsequently increases its oral bioavailability. Ergotamine is known to precipitate angina pectoris. Therefore, patients receiving sublingual nitroglycerin should avoid ergotamine and related drugs or be monitored for symptoms of ergotism if this is not possible.

8 Use In Specific Populations

8.1 PregnancyPregnancy Category C -Animal teratology studies have not been conducted with nitroglycerin lingual spray. Teratology studies in rats and rabbits, however, were conducted with topically applied nitroglycerin ointment at doses up to 80 mg/kg/day and 240 mg/kg/day, respectively.No toxic effects on dams or fetuses were seen at any dose tested. A teratogenicity study was conducted in the third mating of F0 generation female rats administered dietary nitroglycerin for gestation day 6 to day 15 at dose levels used in the 3-generation reproduction study. In offspring of the high-dose nitroglycerin group, increased incidence of diaphragmatic hernias and decreased hyoid bone ossification were seen. The latter finding probably reflects delayed development rather than a potential teratogenic effect, thus indicating no clear evidence of teratogenicity of nitroglycerin. There are no adequate and well-controlled studies in pregnant women. Nitroglycerin should be given to pregnant women only if clearly needed.8.3 Nursing MothersIt is not known whether nitroglycerin is excreted in human milk.8.4 Pediatric UseSafety and effectiveness of nitroglycerin in pediatric patients have not been established.8.5 Geriatric UseClinical studies did not include sufficient numbers of subjects aged 65 and over to determine whether they respond differently from younger subjects. Other reported clinical experience has not identified differences in responses between elderly (greater than or equal to 65 years) and younger (less than 65 years) patients. In general, dose selection for an elderly patient should start at the low end of the dosing range, reflecting the greater frequency of decreased hepatic, renal, or cardiac function, and of concomitant disease or other drug therapy.

10 Overdosage

10.1 Signs and symptoms, methemoglobinemiaNitrate overdosage may result in: severe hypotension, persistent throbbing headache, vertigo, palpitation, visual disturbance, flushing and perspiring skin (later becoming cold and cyanotic), nausea and vomiting (possibly with colic and even bloody diarrhea), syncope (especially in the upright posture), methemoglobinemia with cyanosis and anorexia, initial hyperpnea, dyspnea and slow breathing, slow pulse (dicrotic and intermittent), heart block, increased intracranial pressure with cerebral symptoms of confusion and moderate fever, paralysis and coma followed by clonic convulsions, and possibly death due to circulatory collapse.Case reports of clinically significant methemoglobinemia are rare at conventional doses of organic nitrates. The formation of methemoglobin is dose-related and in the case of genetic abnormalities of hemoglobin that favor methemoglobin formation, even conventional doses of organic nitrates could produce harmful concentrations of methemoglobin.10.2 Treatment of overdosageAs hypotension associated with nitroglycerin overdose is the result of venodilatation and arterial hypovolemia, prudent therapy in this situation should be directed toward increase in central fluid volume. No specific antagonist to the vasodilator effects of nitroglycerin is known. Keep the patient recumbent in a shock position and comfortably warm. Passive movement of the extremities may aid venous return. Intravenous infusion of normal saline or similar fluid may also be necessary. Administer oxygen and artificial ventilation, if necessary. If methemoglobinemia is present, administration of methylene blue (1% solution), 1-2 mg per kilogram of body weight intravenously, may be required unless the patient is known to have G-6-PD deficiency. If an excessive quantity of Nitroglycerin Lingual Spray has been recently swallowed gastric lavage may be of use.As epinephrine is ineffective in reversing the severe hypotensive events associated with overdosage, it is not recommended for resuscitation.

11 Description

Nitroglycerin, an organic nitrate, is a vasodilator which has effects on both arteries and veins. The chemical name for nitroglycerin is 1,2,3-propanetriol trinitrate (C3H5N3O9). The compound has a molecular weight of 227.09. The chemical structure is:Nitroglycerin Lingual Spray (nitroglycerin lingual spray 400 mcg) is a metered dose spray containing nitroglycerin. This product delivers nitroglycerin (400 mcg per spray, 60 or 200 metered sprays) in the form of spray droplets onto or under the tongue. Inactive ingredients: medium-chain triglycerides, dehydrated alcohol, medium-chain partial glycerides, peppermint oil.

12 Clinical Pharmacology

12.1 Mechanism of actionNitroglycerin forms free radical nitric oxide (NO), which activates guanylate cyclase, resulting in an increase of guanosine 3',5'-monophosphate (cyclic GMP) in smooth muscle and other tissues. This eventually leads to dephosphorylation of myosin light chains, which regulates the contractile state in smooth muscle and results in vasodilatation.12.2 PharmacodynamicsThe principal pharmacological action of nitroglycerin is relaxation of vascular smooth muscle. Although venous effects predominate, nitroglycerin produces, in a dose-related manner, dilation of both arterial and venous beds. Dilation of the postcapillary vessels, including large veins, promotes peripheral pooling of blood, decreases venous return to the heart, and reduces left ventricular end-diastolic pressure (preload). Nitroglycerin also produces arteriolar relaxation, thereby reducing peripheral vascular resistance and arterial pressure (after load), and dilates large epicardial coronary arteries; however, the extent to which this latter effect contributes to the relief of exertional angina is unclear.Therapeutic doses of nitroglycerin may reduce systolic, diastolic and mean arterial blood pressure. Effective coronary perfusion pressure is usually maintained, but can be compromised if blood pressure falls excessively or increased heart rate decreases diastolic filling time.Elevated central venous and pulmonary capillary wedge pressures, and pulmonary and systemic vascular resistance are also reduced by nitroglycerin therapy. Heart rate is usually slightly increased, presumably a reflex response to the fall in blood pressure. Cardiac index may be increased, decreased, or unchanged. Myocardial oxygen consumption or demand (as measured by the pressure-rate product, tension-time index, and stroke-work index) is decreased and a more favorable supply-demand ratio can be achieved. Patients with elevated left ventricular filling pressure and increased systemic vascular resistance in association with a depressed cardiac index are likely to experience an improvement in cardiac index. In contrast, when filling pressures and cardiac index are normal, cardiac index may be slightly reduced following nitroglycerin administration.12.3 PharmacokineticsA liver reductase enzyme is of primary importance in the metabolism of nitroglycerin to glycerol di- and mononitrate metabolites and ultimately to glycerol and organic nitrate. Known sites of extrahepatic metabolism include red blood cells and vascular walls. In addition to nitroglycerin, 2 major metabolites, 1,2- and 1,3-dinitroglycerin are found in plasma. The mean elimination half-life of both 1,2- and 1,3-dinitroglycerin is about 40 minutes. The 1,2- and 1,3-dinitroglycerin metabolites have been reported to possess some pharmacological activity, whereas the glycerol mononitrate metabolites of nitroglycerin are essentially inactive. Higher plasma concentrations of the dinitro metabolites, with their nearly 8-fold longer elimination half-lives, may contribute significantly to the duration of pharmacologic effect.In a pharmacokinetic study when a single 0.8 mg dose of nitroglycerin lingual spray was administered to healthy volunteers (n = 24), the mean Cmax and tmax were 1.041 pg/mL and 7.5 minutes, respectively. Additionally, in these subjects the mean area under the curve (AUC) was 12.769 pg/mL · min.The volume of distribution of nitroglycerin following intravenous administration is 3.3 L/kg.Drug interactionsAspirin: Coadministration of nitroglycerin with high dose aspirin (1000 mg) results in increased exposure to nitroglycerin. The vasodilatory and hemodynamic effects of nitroglycerin may be enhanced by concomitant administration of nitroglycerin with high dose aspirin.Tissue-type plasminogen activator (t-PA): Concomitant administration of t-PA and intravenous nitroglycerin has been shown to reduce plasma levels of t-PA and its thrombolytic effect.

13 Nonclinical Toxicology

13.1 Carcinogenesis, Mutagenesis, Impairment of FertilityAnimal carcinogenesis studies with sublingual nitroglycerin have not been performed.Rats receiving up to 434 mg/kg/day of dietary nitroglycerin for 2 years developed dose-related fibrotic and neoplastic changes in liver, including carcinomas, and interstitial cell tumors in testes. At high dose, the incidences of hepatocellular carcinomas in both sexes were 52% vs. 0% in controls, and incidences of testicular tumors were 52% vs. 8% in controls.Lifetime dietary administration of up to 1058 mg/kg/day of nitroglycerin was not tumorigenic in mice.Nitroglycerin was weakly mutagenic in Ames tests performed in two different laboratories. There was no evidence of mutagenicity in an in vivo dominant lethal assay with male rats treated with doses up to about 363 mg/kg/day, p.o., or in in vitro cytogenic tests in rat and dog tissues and for chromosomal aberration in Chinese hamster ovary cells.In a three-generation reproduction study, rats received dietary nitroglycerin at doses up to about 434 mg/kg/day for six months prior to mating of the F0 generation with treatment continuing through successive F1 and F2 generations. The high dose was associated with decreased feed intake and body weight gain in both sexes at all matings. No specific effect on the fertility of the F0 generation was seen. Infertility noted in subsequent generations, however, was attributed to increased interstitial cell tissue and aspermatogenesis in the high-dose males. In this three-generation study there was no clear evidence of teratogenicity.

14 Clinical Studies

In a randomized, double-blind single-dose, 5-period cross-over study in 51 patients with exertional angina pectoris significant dose-related increases in exercise tolerance, time to onset of angina and ST-segment depression were seen following doses of 0.2, 0.4, 0.8 and 1.6 mg of nitroglycerin delivered by metered pumpspray as compared to placebo.The drug showed a profile of mild to moderate adverse events.

16 How Supplied/Storage & Handling

NITROGLYCERIN LINGUAL SPRAY is supplied in the following dosage forms.

NDC 51662-1423-1

NITROGLYCERIN LINGUAL SPRAY 400mcg PER SPRAY 60 METERED SPRAYS 4.9g NET CONTENTS UNBOXED
HF Acquisition Co LLC, DBA HealthFirst

Mukilteo, WA 98275
Also supplied in the following manufacture supplied dosage formsEach box of Nitroglycerin Lingual Spray contains one glass bottle coated with orange transparent plastic which assists in containing the glass and medication should the bottle be shattered. Each bottle contains 4.9 g or 12 g (Net Content) of nitroglycerin lingual spray which will deliver 60 or 200 metered sprays containing 400 mcg of nitroglycerin per spray after priming.Nitroglycerin Lingual Spray is available as:•

60-dose (4.9 g) single bottle NDC 45802- 210-01



200-dose (12 g) single bottle NDC 45802- 210-02
Store at 20-25°C (68-77°F) [see USP Controlled Room Temperature].Note: Nitroglycerin Lingual Spray contains 20% alcohol. Do not forcefully open or burn container after use. Do not spray toward flames.Rx Only

17 Patient Counseling Information

Advise the patient to read the FDA-approved patient labeling (Instructions for Use).Made in IsraelManufactured by PerrigoYeruham 80500, IsraelDistributed ByPerrigo®Allegan, MI 49010 • www.perrigo.comRev 04-15: 8A500 RC J3

Patient Counseling Information

Instructions for UseNitroglycerin Lingual SprayRead this Instructions for Use before you start using Nitroglycerin Lingual Spray and each time you get your prescription refilled. There may be new information. This information does not take the place of talking to your healthcare provider about your medical condition or your treatment.Important information:•

Nitroglycerin Lingual Spray is for use onto or under the tongue. Do not inhale Nitroglycerin Lingual Spray.



A dose of Nitroglycerin Lingual Spray may be either 1 or 2 sprays. Follow your healthcare provider’s instructions about how many sprays you should use for each dose. Doses should be separated by approximately 5 minutes.



You should not use more than 3 sprays of Nitroglycerin Lingual Spray within 15 minutes.



Get emergency medical help right away if you still have chest pain after using a total of 3 sprays of Nitroglycerin Lingual Spray.
Nitroglycerin Lingual Spray parts:FIGURE AHow should I use Nitroglycerin Lingual Spray?•

It is best to use Nitroglycerin Lingual Spray while you are resting and in a sitting position.



Do not shake the Nitroglycerin Lingual Spray container.
Priming Nitroglycerin Lingual Spray:Before you use Nitroglycerin Lingual Spray for the first time, you must prime it. To prime your Nitroglycerin Lingual Spray, follow the steps below:Step 1. Remove the plastic cap from the container.(See Figure B)FIGURE BStep 2. Hold the container upright and facing away from yourself and others. Press down on the top of the grooved button 5 times.(See Figure C)FIGURE C•

Your Nitroglycerin Lingual Spray is now primed. You are ready to give your first dose.



If you do not use your Nitroglycerin Lingual Spray within 6 weeks, you will need to prime it again by pressing down on the top of the grooved button 1 time.



If you do not use your Nitroglycerin Lingual Spray within 3 months, you will need to re-prime it by pressing down on the top of the grooved button up to 5 times.
Giving a dose of Nitroglycerin Lingual Spray:Step 3. Hold your Nitroglycerin Lingual Spray container upright with your index finger on top of the grooved button.Step 4. Open your mouth and bring the Nitroglycerin Lingual Spray container as close to your mouth as possible.Step 5. Press down on the top of the grooved button firmly with your index finger to release the spray onto or under your tongue. (See Figure D). The grooved button can help you make sure the canister is turned to the correct position if you are administering the spray in the dark.FIGURE DStep 6. Release the grooved button and close your mouth right away. Avoid swallowing right after using Nitroglycerin Lingual Spray. Do not spit out Nitroglycerin Lingual Spray or rinse your mouth for 5 to 10 minutes after using Nitroglycerin Lingual Spray.Step 7. If a second dose of Nitroglycerin Lingual Spray is needed, repeat Steps 3 through 6 above.Step 8. Replace the plastic cap.Check the level of the fluid in your Nitroglycerin Lingual Spray container regularly.•

Check the container in an upright position.



The end of the center tube should be covered by the fluid in the Nitroglycerin Lingual Spray container. If the level of the fluid falls below the end of the center tube, sprays will not provide enough Nitroglycerin Lingual Spray.



Replace your Nitroglycerin Lingual Spray container before the fluid level falls below the end of the center tube.
How should I store Nitroglycerin Lingual Spray?•

Store Nitroglycerin Lingual Spray at room temperature 20-25°C (68-77°F) [see USP Controlled Room Temperature].



Do not forcefully open or burn the Nitroglycerin Lingual Spray container after use.



Do not spray Nitroglycerin Lingual Spray toward flames.
Keep Nitroglycerin Lingual Spray and all medicines out of the reach of children.This Instructions for Use has been approved by the U.S. Food and Drug Administration.Made in IsraelManufactured by PerrigoYeruham 80500, IsraelDistributed ByPerrigo®Allegan, MI 49010 • www.perrigo.comRev 04-15: 8A500 RC J3

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