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Adderall

NDC 57844-110 · 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 (2.5 mg/1)
AMPHETAMINE SULFATE (2.5 mg/1)
DEXTROAMPHETAMINE SACCHARATE (2.5 mg/1)
DEXTROAMPHETAMINE SULFATE (2.5 mg/1)
Marketing started20140203
Package count1

External sources

Source: openFDA. Public-domain (CC0).