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Dextroamphetamine Sulfate

NDC 75826-124 · HUMAN PRESCRIPTION DRUG · TABLET

Labeler / ManufacturerWinder Laboratories LLC
Marketing categoryAbbreviated NDA (generic) · App ANDA212160
Dosage form / routeTABLET · ORAL
Active ingredientsDEXTROAMPHETAMINE SULFATE (15 mg/1)
Marketing started20211206
Package count2

External sources

Source: openFDA. Public-domain (CC0).