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Dexmethylphenidate hydrochloride

NDC 57664-376 · HUMAN PRESCRIPTION DRUG · TABLET

Labeler / ManufacturerSun Pharmaceutical Industries, Inc.
Marketing categoryAbbreviated NDA (generic) · App ANDA201231
Dosage form / routeTABLET · ORAL
Active ingredientsDEXMETHYLPHENIDATE HYDROCHLORIDE (2.5 mg/1)
Marketing started20130926
Package count5

External sources

Source: openFDA. Public-domain (CC0).