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Amphetamine Sulfate

NDC 69238-1564 · HUMAN PRESCRIPTION DRUG · TABLET

Generic nameAmphetamine
Labeler / ManufacturerAmneal Pharmaceuticals NY LLC
Marketing categoryAbbreviated NDA (generic) · App ANDA211139
Dosage form / routeTABLET · ORAL
Active ingredientsAMPHETAMINE SULFATE (10 mg/1)
Marketing started20180928
Package count1

External sources

Source: openFDA. Public-domain (CC0).