FDA NDC Directory · JSON-LD · Markdown

Dextroamphetamine saccharate, amphetamine aspartate, dextroamphetamine sulfate, and amphetamine sulfate

NDC 57664-641 · HUMAN PRESCRIPTION DRUG · TABLET

Generic nameDextroamphetamine saccharate, Amphetamine aspartate, Dextroamphetamine sulfate, and Amphetamine sulfate
Labeler / ManufacturerSun Pharmaceutical Industries, Inc.
Marketing categoryAbbreviated NDA (generic) · App ANDA040480
Dosage form / routeTABLET · ORAL
Active ingredientsAMPHETAMINE ASPARTATE (1.25 mg/1)
AMPHETAMINE SULFATE (1.25 mg/1)
DEXTROAMPHETAMINE SACCHARATE (1.25 mg/1)
DEXTROAMPHETAMINE SULFATE (1.25 mg/1)
Marketing started20030909
Package count1

External sources

Source: openFDA. Public-domain (CC0).