FDA NDC Directory · JSON-LD · Markdown

AMPHETAMINE SULFATE

NDC 72162-1368 · HUMAN PRESCRIPTION DRUG · TABLET

Generic nameamphetamine sulfate
Labeler / ManufacturerBryant Ranch Prepack
Marketing categoryAbbreviated NDA (generic) · App ANDA211861
Dosage form / routeTABLET · ORAL
Active ingredientsAMPHETAMINE SULFATE (5 mg/1)
Marketing started20200402
Package count1

External sources

Source: openFDA. Public-domain (CC0).