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METHYLPHENIDATE HYDROCHLORIDE

NDC 0115-1800 · HUMAN PRESCRIPTION DRUG · TABLET

Labeler / ManufacturerAmneal Pharmaceuticals of New York LLC
Marketing categoryAbbreviated NDA (generic) · App ANDA091159
Dosage form / routeTABLET · ORAL
Active ingredientsMETHYLPHENIDATE HYDROCHLORIDE (5 mg/1)
Marketing started20140407
Package count1

External sources

Source: openFDA. Public-domain (CC0).