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Methylphenidate Hydrochloride

NDC 31722-952 · HUMAN PRESCRIPTION DRUG · TABLET, EXTENDED RELEASE

Labeler / ManufacturerCamber Pharmaceuticals, Inc.
Marketing categoryAbbreviated NDA (generic) · App ANDA211009
Dosage form / routeTABLET, EXTENDED RELEASE · ORAL
Active ingredientsMETHYLPHENIDATE HYDROCHLORIDE (18 mg/1)
Marketing started20190903
Package count1

External sources

Source: openFDA. Public-domain (CC0).