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Adderall

NDC 57844-117 · HUMAN PRESCRIPTION DRUG · TABLET

Generic nameDextroamphetamine Saccharate, Amphetamine Aspartate, Dextroamphetamine Sulfate, and Amphetamine Sulfate
Labeler / ManufacturerTeva Pharmaceuticals USA, Inc.
Marketing categoryAbbreviated NDA (generic) · App ANDA040422
Dosage form / routeTABLET · ORAL
Active ingredientsAMPHETAMINE ASPARTATE MONOHYDRATE (1.875 mg/1)
AMPHETAMINE SULFATE (1.875 mg/1)
DEXTROAMPHETAMINE SACCHARATE (1.875 mg/1)
DEXTROAMPHETAMINE SULFATE (1.875 mg/1)
Marketing started20150303
Package count1

External sources

Source: openFDA. Public-domain (CC0).