FDA NDC Directory · JSON-LD · Markdown

Benzphetamine Hydrochloride

NDC 42806-081 · HUMAN PRESCRIPTION DRUG · TABLET, FILM COATED

Labeler / ManufacturerEpic Pharma, LLC
Marketing categoryAbbreviated NDA (generic) · App ANDA090346
Dosage form / routeTABLET, FILM COATED · ORAL
Active ingredientsBENZPHETAMINE HYDROCHLORIDE (50 mg/1)
Marketing started20151216
Package count3

External sources

Source: openFDA. Public-domain (CC0).