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Naftifine Hydrochloride

NDC 51672-1368 · HUMAN PRESCRIPTION DRUG · CREAM

Labeler / ManufacturerSun Pharmaceutical Industries, Inc.
Marketing categoryAbbreviated NDA (generic) · App ANDA206901
Dosage form / routeCREAM · TOPICAL
Active ingredientsNAFTIFINE HYDROCHLORIDE (20 mg/g)
Marketing started20160106
Package count3

External sources

Source: openFDA. Public-domain (CC0).