51672-1376 : Naftifine Hydrochloride 20 mg/g Topical Gel


NDC: 51672-1376
Labeler: Taro Pharmaceuticals U.S.a., Inc.
Product Type: Human Prescription Drug
Drug Name:  Naftifine Hydrochloride
Dosage Form: Topical Gel
Application #: ANDA208201
Rev. Date: 


NDC Package Codes:

  • 51672-1376-3: 1 TUBE IN 1 CARTON (51672‑1376‑3) > 60 G IN 1 TUBE
  • 51672-1376-6: 1 TUBE IN 1 CARTON (51672‑1376‑6) > 45 G IN 1 TUBE

Active Ingredients:

  • Naftifine Hydrochloride

Dosage Strength:

  • 20 mg/g

Pharmaceutical Classes:

  • Allylamine [CS]
  • Allylamine Antifungal [EPC]

Related Products:

Based on records with the same trade name.
  • 51672-1362 Naftifine Hydrochloride 10 mg/g Topical Cream by Taro Pharmaceuticals U.S.a., Inc.
  • 51672-1368 Naftifine Hydrochloride 20 mg/g Topical Cream by Taro Pharmaceuticals U.S.a., Inc.
  • 0115-1510 Naftifine Hydrochloride 10 mg/g Topical Gel by Amneal Pharmaceuticals of New York LLC
  • 0115-1512 Naftifine Hydrochloride 20 mg/g Topical Cream by Impax Generics
  • 40085-201 Naftifine Hydrochloride 1 mg/g Topical Cream by Renaissance Pharma, Inc
  • 40085-203 Naftifine Hydrochloride 20 mg/g Topical Cream by Renaissance Pharma, Inc
  • 70700-161 Naftifine Hydrochloride 20 mg/g Topical Cream by Xiromed, LLC

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Note: The RxChat NDC Database uses publicly available data from the FDA and the U.S. National Library of Medicine (NLM); The NLM is not responsible for the data presented and does not endorse or recommend this or any other product. While we make every effort to ensure that the information presented is accurate, you should assume that all results are unvalidated. To report any errors or inconsistencies please contact us.