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Methylphenidate Hydrochloride

NDC 13811-708 · HUMAN PRESCRIPTION DRUG · TABLET, EXTENDED RELEASE

Generic nameMethylphenidate hydrochloride
Labeler / ManufacturerTrigen Laboratories, LLC
Marketing categoryAbbreviated NDA (generic) · App ANDA205327
Dosage form / routeTABLET, EXTENDED RELEASE · ORAL
Active ingredientsMETHYLPHENIDATE HYDROCHLORIDE (36 mg/1)
Marketing started20170814
Package count1

External sources

Source: openFDA. Public-domain (CC0).