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DEXTROAMPHETAMINE SACCHARATE, AMPHETAMINE ASPARTATE, DEXTROAMPHETAMINE SULFATE AND AMPHETAMINE SULFATE

NDC 11534-191 · HUMAN PRESCRIPTION DRUG · TABLET

Generic namedextroamphetamine saccharate, amphetamine aspartate, dextroamphetamine sulfate and amphetamine sulfate
Labeler / ManufacturerSUNRISE PHARMACEUTICAL, INC.
Marketing categoryAbbreviated NDA (generic) · App ANDA209799
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 started20180704
Package count2

External sources

Source: openFDA. Public-domain (CC0).