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Naftifine Hydrochloride

NDC 51672-1376 · HUMAN PRESCRIPTION DRUG · GEL

Labeler / ManufacturerSun Pharmaceutical Industries, Inc.
Marketing categoryAbbreviated NDA (generic) · App ANDA208201
Dosage form / routeGEL · TOPICAL
Active ingredientsNAFTIFINE HYDROCHLORIDE (20 mg/g)
Marketing started20230401
Package count2

External sources

Source: openFDA. Public-domain (CC0).