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Methylphenidate Hydrochloride

NDC 64980-221 · HUMAN PRESCRIPTION DRUG · TABLET, CHEWABLE

Labeler / ManufacturerRising Pharma Holdings, Inc.
Marketing categoryAbbreviated NDA (generic) · App ANDA205756
Dosage form / routeTABLET, CHEWABLE · ORAL
Active ingredientsMETHYLPHENIDATE HYDROCHLORIDE (2.5 mg/1)
Marketing started20181218
Package count1

External sources

Source: openFDA. Public-domain (CC0).