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Ritalin

NDC 0078-0441 · HUMAN PRESCRIPTION DRUG · TABLET

Generic namemethylphenidate hydrochloride
Labeler / ManufacturerNovartis Pharmaceuticals Corporation
Marketing categoryNew Drug Application (innovator) · App NDA010187
Dosage form / routeTABLET · ORAL
Active ingredientsMETHYLPHENIDATE HYDROCHLORIDE (20 mg/1)
Marketing started19551231
Marketing ended20260831
Package count1

External sources

Source: openFDA. Public-domain (CC0).