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Dextroamphetamine Saccharate, Amphetamine Aspartate, Dextroamphetamine Sulfate and Amphetamine Sulfate

NDC 64850-503 · HUMAN PRESCRIPTION DRUG · TABLET

Labeler / ManufacturerElite Laboratories, Inc.
Marketing categoryAbbreviated NDA (generic) · App ANDA211352
Dosage form / routeTABLET · ORAL
Active ingredientsAMPHETAMINE ASPARTATE MONOHYDRATE (3.125 mg/1)
AMPHETAMINE SULFATE (3.125 mg/1)
DEXTROAMPHETAMINE SACCHARATE (3.125 mg/1)
DEXTROAMPHETAMINE SULFATE (3.125 mg/1)
Marketing started20221229
Package count3

External sources

Source: openFDA. Public-domain (CC0).