FDA NDC Directory · JSON-LD · Markdown

Amphetamine Sulfate

NDC 13107-260 · HUMAN PRESCRIPTION DRUG · TABLET

Labeler / ManufacturerAurolife Pharma, LLC
Marketing categoryAbbreviated NDA (generic) · App ANDA211639
Dosage form / routeTABLET · ORAL
Active ingredientsAMPHETAMINE SULFATE (10 mg/1)
Marketing started20190131
Package count1

External sources

Source: openFDA. Public-domain (CC0).