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LISDEXAMFETAMINE DIMESYLATE

NDC 57664-083 · HUMAN PRESCRIPTION DRUG · TABLET, CHEWABLE

Labeler / ManufacturerSun Pharmaceutical Industries, Inc.
Marketing categoryAbbreviated NDA (generic) · App ANDA214134
Dosage form / routeTABLET, CHEWABLE · ORAL
Active ingredientsLISDEXAMFETAMINE DIMESYLATE (10 mg/1)
Marketing started20230825
Package count1

External sources

Source: openFDA. Public-domain (CC0).