FDA NDC Directory · JSON-LD · Markdown

AMPHETAMINE SULFATE

NDC 0527-2524 · HUMAN PRESCRIPTION DRUG · TABLET

Generic nameamphetamine sulfate
Labeler / ManufacturerLannett Company, Inc.
Marketing categoryAbbreviated NDA (generic) · App ANDA212901
Dosage form / routeTABLET · ORAL
Active ingredientsAMPHETAMINE SULFATE (5 mg/1)
Marketing started20200525
Package count1

External sources

Source: openFDA. Public-domain (CC0).