NDC 51672-4215 Metronidazole

Metronidazole

NDC Product Code 51672-4215

NDC Code: 51672-4215

Proprietary Name: Metronidazole 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: Metronidazole 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.

NDC Code Structure

  • 51672 - Taro Pharmaceuticals U.s.a., Inc.
    • 51672-4215 - Metronidazole

NDC 51672-4215-3

Package Description: 1 TUBE in 1 CARTON > 60 g in 1 TUBE

NDC 51672-4215-6

Package Description: 1 TUBE in 1 CARTON > 45 g in 1 TUBE

NDC 51672-4215-9

Package Description: 1 BOTTLE, PUMP in 1 CARTON > 55 g in 1 BOTTLE, PUMP

NDC Product Information

Metronidazole with NDC 51672-4215 is a a human prescription drug product labeled by Taro Pharmaceuticals U.s.a., Inc.. The generic name of Metronidazole is metronidazole. The product's dosage form is gel and is administered via topical form.

Labeler Name: Taro Pharmaceuticals U.s.a., Inc.

Dosage Form: Gel - A semisolid3 dosage form that contains a gelling agent to provide stiffness to a solution or a colloidal dispersion.4 A gel may contain suspended particles.

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.

Metronidazole 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.

  • METRONIDAZOLE 10 mg/g

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)
  • EDETATE DISODIUM (UNII: 7FLD91C86K)
  • POLYETHYLENE GLYCOL 400 (UNII: B697894SGQ)
  • PROPYLENE GLYCOL (UNII: 6DC9Q167V3)
  • WATER (UNII: 059QF0KO0R)
  • SORBIC ACID (UNII: X045WJ989B)

Administration Route(s)

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

  • Topical - Administration to a particular spot on the outer surface of the body. The E2B term TRANSMAMMARY is a subset of the term TOPICAL.

Pharmacological Class(es)

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

  • Nitroimidazole Antimicrobial - [EPC] (Established Pharmacologic Class)
  • Nitroimidazoles - [CS]

Product Labeler Information

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

Labeler Name: Taro Pharmaceuticals U.s.a., Inc.
Labeler Code: 51672
FDA Application Number: ANDA204651 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: 04-09-2019 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: 12-31-2020 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

Metronidazole Topical

Metronidazole Topical is pronounced as (me troe ni' da zole)

Why is metronidazole topical medication prescribed?
Metronidazole is used to treat rosacea (a skin disease that causes redness, flushing, and pimples on the face). Metronidazole is in a class of medications called nitroimi...
[Read More]

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Metronidazole 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

Metronidazole Gel USP, 1% is indicated for the topical treatment of inflammatory lesions of rosacea.

2 Dosage And Administration

Apply and rub in a thin film of metronidazole once daily to affected area(s).A gentle cleanser should be used before the application of metronidazole.Cosmetics may be applied after the application of metronidazole. Not for oral, ophthalmic or intravaginal use.

3 Dosage Forms And Strengths

Gel, 1%. Metronidazole is a colorless to slightly yellow gel. Each gram of metronidazole contains 10 mg (1%) of metronidazole.

4 Contraindications

Metronidazole Gel USP, 1% is contraindicated in patients with a history of hypersensitivity to metronidazole or to any other ingredient in the formulation.

5.1 Neurologic Disease

Peripheral neuropathy, characterized by numbness or paresthesia of an extremity has been reported in patients treated with systemic metronidazole. Although not evident in clinical trials for topical metronidazole, peripheral neuropathy has been reported with the post approval use. The appearance of abnormal neurologic signs should prompt immediate reevaluation of metronidazole therapy. Metronidazole should be administered with caution to patients with central nervous system diseases.

5.2 Blood Dyscrasias

Metronidazole is a nitroimidazole; use with care in patients with evidence of, or history of, blood dyscrasia.

5.3 Contact Dermatitis

Irritant and allergic contact dermatitis have been reported. If dermatitis occurs, patients may need to discontinue use.

5.4 Eye Irritation

Topical metronidazole has been reported to cause tearing of the eyes. Avoid contact with the eyes.

6.1 Clinical Trials Experience

Because 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 practice.In a controlled clinical trial, 557 patients used metronidazole gel USP, 1% and 189 patients used the gel vehicle once daily for up to 10 weeks. The following table summarizes selected adverse reactions that occurred at a rate of ≥1%:Table 1: Adverse Reactions That Occurred at a Rate of ≥1%System Organ Class/Preferred TermMetronidazole Gel USP, 1%Gel VehicleN=557N=189Patients with at least one AE    Number (%) of Patients186 (33.4)51 (27.0)Infections and infestations76 (13.6)28 (14.8)  Bronchitis6 (1.1)3 (1.6)  Influenza8 (1.4)1 (0.5)  Nasopharyngitis17 (3.1)8 (4.2)  Sinusitis8 (1.4)3 (1.6)  Upper respiratory tract infection14 (2.5)4 (2.1)  Urinary tract infection6 (1.1)1 (0.5)  Vaginal mycosis1 (0.2)2 (1.1)Musculoskeletal and connective tissue disorders19 (3.4)5 (2.6)  Back pain3 (0.5)2 (1.1)Neoplasms4 (0.7)2 (1.1)  Basal cell carcinoma1 (0.2)2 (1.1)Nervous system disorders18 (3.2)3 (1.6)  Headache12 (2.2)1 (0.5)Respiratory, thoracic and mediastinal disorders22 (3.9)5 (2.6)  Nasal congestion6 (1.1)3 (1.6)Skin and subcutaneous tissue disorders36 (6.5)12 (6.3)  Contact dermatitis7 (1.3)1 (0.5)  Dry skin6 (1.1)3 (1.6)Vascular disorders8 (1.4)1 (0.5)  Hypertension6 (1.1)1 (0.5)Table 2: Local Cutaneous Signs and Symptoms of Irritation That Were Worse Than BaselineMetronidazole Gel USP, 1%Gel VehicleSign/SymptomN=544N=184Dryness138 (25.4)63 (34.2)  Mild93 (17.1)41 (22.3)  Moderate42 (7.7)20 (10.9)  Severe3 (0.6)2 (1.1)Scaling134 (24.6)60 (32.6)  Mild88 (16.2)32 (17.4)  Moderate43 (7.9)27 (14.7)  Severe3 (0.6)1 (0.5)Pruritus86 (15.8)35 (19.0)  Mild53 (9.7)21 (11.4)  Moderate27 (5.0)13 (7.1)  Severe6 (1.1)1 (0.5)Stinging/burning56 (10.3)28 (15.2)  Mild39 (7.2)18 (9.8)  Moderate7 (1.3)9 (4.9)  Severe10 (1.8)1 (0.5)The following additional adverse experiences have been reported with the topical use of metronidazole: skin irritation, transient redness, metallic taste, tingling or numbness of extremities, and nausea.

6.2 Post Marketing Experience

The following adverse reaction has been identified during post approval use of topical metronidazole: peripheral neuropathy. Because this reaction is reported voluntarily from a population of uncertain size, it is not always possible to reliably estimate the frequency or establish a causal relationship to drug exposure.

7 Drug Interactions

Oral metronidazole has been reported to potentiate the anticoagulant effect of coumarin and warfarin, resulting in a prolongation of prothrombin time. Drug interactions should be kept in mind when metronidazole is prescribed for patients who are receiving anticoagulant treatment, although they are less likely to occur with topical metronidazole administration because of low absorption.

Teratogenic Effects

Teratogenic Effects: Pregnancy Category B.There are no adequate and well-controlled studies with the use of metronidazole in pregnant women.Metronidazole crosses the placental barrier and enters the fetal circulation rapidly. No fetotoxicity was observed after oral administration of metronidazole in rats or mice at 200 and 20 times, respectively, the expected clinical dose. However, oral metronidazole has shown carcinogenic activity in rodents. Because animal reproduction studies are not always predictive of human response, metronidazole should be used during pregnancy only if clearly needed.

8.3 Nursing Mothers

After oral administration, metronidazole is secreted in breast milk in concentrations similar to those found in the plasma. Even though blood levels taken after topical metronidazole application are significantly lower than those achieved after oral metronidazole a decision should be made whether to discontinue nursing or to discontinue the drug, taking into account the importance of the drug to the mother and the risk to the infant.

8.4 Pediatric Use

Safety and effectiveness in pediatric patients have not been established.

8.5 Geriatric Use

Sixty-six subjects aged 65 years and older were treated with metronidazole gel USP, 1% in the clinical study. No overall differences in safety or effectiveness were observed between these subjects and younger subjects, and other reported clinical experience has not identified differences in responses between the elderly and younger patients, but greater sensitivity of some older individuals cannot be ruled out.

10 Overdosage

There are no reported human experiences with overdosage of metronidazole. Topically applied metronidazole can be absorbed in sufficient amount to produce systemic effects.

11 Description

Metronidazole Gel USP, 1% contains metronidazole, USP. Chemically, metronidazole is 2-methyl-5-nitro-1 H-imidazole- 1-ethanol. The molecular formula for metronidazole is C6H9N3O3. It has the following structural formula:Metronidazole has a molecular weight of 171.16. It is a white to pale yellow crystalline powder. It is slightly soluble in alcohol and has solubility in water of 10 mg/mL at 20°C. Metronidazole belongs to the nitroimidazole class of compounds. Metronidazole is a colorless to slightly yellow gel; each gram contains 10 mg of metronidazole in a base of alcohol (9.3% w/w), edetate disodium, hydroxyethylcellulose, polyethylene glycol 400, propylene glycol, sorbic acid, and purified water.

12.1 Mechanism Of Action

The mechanism of action of metronidazole in the treatment of rosacea is unknown.

12.2 Pharmacodynamics

The pharmacodynamics of metronidazole in association with the treatment of rosacea are unknown.

12.3 Pharmacokinetics

Topical administration of a one gram dose of metronidazole to the face of 13 patients with moderate to severe rosacea once daily for 7 days resulted in a mean ± SD Cmax of metronidazole of 32 ± 9 ng/mL. The mean ± SD AUC(0-24) was 595 ± 154 ng*hr/mL.The mean Cmax and AUC(0-24) are less than 1% of the value reported for a single 250 mg oral dose of metronidazole. The time to maximum plasma concentration (Tmax) was 6 to 10 hours after topical application.

13.1 Carcinogenesis, Mutagenesis, Impairment Of Fertility

Metronidazole has shown evidence of carcinogenic activity in a number of studies involving chronic, oral administration in mice and rats, but not in studies involving hamsters.In several long-term studies in mice, oral doses of approximately 225 mg/m2/day or greater (approximately 37 times the human topical dose on a mg/m2 basis) were associated with an increase in pulmonary tumors and lymphomas. Several long-term oral studies in the rat have shown statistically significant increases in mammary and hepatic tumors at doses >885 mg/m2/day (144 times the human dose).Metronidazole has shown evidence of mutagenic activity in several in vitro bacterial assay systems. In addition, a dose-related increase in the frequency of micronuclei was observed in mice after intraperitoneal injections. An increase in chromosomal aberrations in peripheral blood lymphocytes was reported in patients with Crohn's disease who were treated with 200 to 1200 mg/day of metronidazole for 1 to 24 months. However, in another study, no increase in chromosomal aberrations in circulating lymphocytes was observed in patients with Crohn's disease treated with the drug for 8 months.In one published study, using albino hairless mice, intraperitoneal administration of metronidazole at a dose of 45 mg/m2/day (approximately 7 times the human topical dose on a mg/m2 basis) was associated with an increase in ultraviolet radiation induced skin carcinogenesis. Neither dermal carcinogenicity nor photocarcinogenicity studies have been performed with metronidazole gel USP, 1% or any marketed metronidazole formulations.

14 Clinical Studies

In a randomized, vehicle-controlled trial, 746 subjects with rosacea were treated with metronidazole gel USP, 1% or gel vehicle once daily for 10 weeks. Most subjects had "moderate" rosacea at baseline. Efficacy was determined by recording reduction in inflammatory lesion counts and success rate in the Investigator Global Assessment (percentage of subjects "clear" and "almost clear" of rosacea at the end of the study). The scale is based on the following definitions:Table 3: Investigator Global Assessment ScaleScoreGradeDefinition0ClearNo signs or symptoms present; at most, mild erythema1Almost ClearVery mild erythema present. Very few small papules/pustules2MildMild erythema. Several small papules/pustules3ModerateModerate erythema. Several small or large papules/pustules, and up to 2 nodules4SevereSevere erythema. Numerous small and/or large papules/pustules, up to several nodulesThe results are shown in the following table:Table 4: Inflammatory Lesion Counts and Global Scores in a Clinical Trial of RosaceaMetronidazole Gel USP, 1%VehicleNResults N(%)NResults N(%)Inflammatory lesions557189Baseline, mean count18.318.4Week-10, mean count8.912.8Reduction9.4 (50.7)5.6 (32.6)Investigator Global Assessment557189Subject clear or almost clear214 (38.42)52 (27.51)Subject with no change159 (28.5)77 (40.7)Subjects treated with metronidazole gel USP, 1% experienced a mean reduction of 9.4 inflammatory lesions in the Week-10 LOCF group, compared to a reduction of 5.6 for those treated with vehicle, or a difference in means of 3.8 lesions.The contribution to efficacy of individual components of the vehicle has not been established.

16 How Supplied/Storage And Handling

Metronidazole Gel USP, 1% is colorless to slightly yellow in color, and supplied as follows:45 g tube - (NDC 51672-4215-6)60 g tube - (NDC 51672-4215-3)55 g pump - (NDC 51672-4215-9)

Storage And Handling

Storage Conditions: Store at 20° to 25°C (68° to 77°F) [see USP Controlled Room Temperature].

17 Patient Counseling Information

  • Patients using Metronidazole Gel USP, 1% should receive the following information and instructions:This medication is to be used as directed.It is for external use only.Avoid contact with the eyes.Cleanse affected area(s) before applying Metronidazole Gel USP, 1%.This medication should not be used for any condition other than that for which it is prescribed.Keep out of reach of children.Patients should report any adverse reaction to their physicians.

Other

Rx OnlyMfd. by: Taro Pharmaceutical Industries Ltd.Haifa Bay, Israel 2624761Dist. by: Taro Pharmaceuticals U.S.A., Inc.Hawthorne, NY 10532Revised: April 201921333-0419-0782

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