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Methylphenidate Hydrochloride

NDC 62037-727 · HUMAN PRESCRIPTION DRUG · TABLET, FILM COATED, EXTENDED RELEASE

Labeler / ManufacturerActavis Pharma, Inc.
Marketing categoryAbbreviated NDA (generic) · App ANDA076655
Dosage form / routeTABLET, FILM COATED, EXTENDED RELEASE · ORAL
Active ingredientsMETHYLPHENIDATE HYDROCHLORIDE (54 mg/1)
Marketing started20190304
Package count1

External sources

Source: openFDA. Public-domain (CC0).