Naftifine Hydrochloride

Sun Pharmaceutical Industries, Inc.🇺🇸 United States

FDA Page

Effective Date: May 25, 2018
Approval ID: a740fc0d-45b3-411f-9dfd-f3d637b8a95f
Products: 1 registered
Version: 5

Regulatory Information

Labeling Type

HUMAN PRESCRIPTION DRUG LABEL

Status

Approved

Full Title

These highlights do not include all the information needed to use NAFTIFINE HYDROCHLORIDE CREAM safely and effectively. See full prescribing information for NAFTIFINE HYDROCHLORIDE CREAM NAFTIFINE HYDROCHLORIDE cream, for topical use Initial U.S. Approval: 1988

Quick Stats

Total Products1

Labelers3

Label Sections25

Regulatory Agency

🇺🇸

U.S. Food and Drug Administration

United States

Data Sources & Disclaimer: Approval information is sourced from official FDA databases. This content is for informational purposes only and does not constitute medical or regulatory advice. Always refer to official FDA websites for the most current information.