FDA NDC Directory · JSON-LD · Markdown

BENZPHETAMINE HYDROCHLORIDE

NDC 10702-040 · HUMAN PRESCRIPTION DRUG · TABLET

Generic namebenzphetamine hydrochloride
Labeler / ManufacturerKVK-TECH, INC
Marketing categoryAbbreviated NDA (generic) · App ANDA090968
Dosage form / routeTABLET · ORAL
Active ingredientsBENZPHETAMINE HYDROCHLORIDE (50 mg/1)
Marketing started20100721
Package count4

External sources

Source: openFDA. Public-domain (CC0).