70700-161 : Naftifine Hydrochloride 20 mg/g Topical Cream


NDC: 70700-161
Labeler: Xiromed, LLC
Product Type: Human Prescription Drug
Drug Name:  Naftifine Hydrochloride
Dosage Form: Topical Cream
Application #: ANDA210038
Rev. Date: 


NDC Package Codes:

  • 70700-161-17: 1 TUBE IN 1 CARTON (70700‑161‑17) > 60 G IN 1 TUBE
  • 70700-161-18: 1 TUBE IN 1 CARTON (70700‑161‑18) > 45 G IN 1 TUBE

Active Ingredients:

  • Naftifine Hydrochloride

Dosage Strength:

  • 20 mg/g

Pharmaceutical Classes:

  • Allylamine Antifungal [EPC]
  • Allylamine [CS]

Related Products:

Based on records with the same trade name.
  • 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
  • 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.
  • 51672-1376 Naftifine Hydrochloride 20 mg/g Topical Gel by Taro Pharmaceuticals U.S.a., Inc.

NDC QR Code

Scan the QR code below to easily reference this data in the future:

NDC 70700-161 QR Code

< Prev: 70700-160Next: 70700-162 >




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.