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METHYLPHENIDATE HYDROCHLORIDE

NDC 70010-042 · HUMAN PRESCRIPTION DRUG · TABLET, EXTENDED RELEASE

Labeler / ManufacturerGranules Pharmaceuticals Inc.
Marketing categoryAbbreviated NDA (generic) · App ANDA210992
Dosage form / routeTABLET, EXTENDED RELEASE · ORAL
Active ingredientsMETHYLPHENIDATE HYDROCHLORIDE (10 mg/1)
Marketing started20181217
Package count2

External sources

Source: openFDA. Public-domain (CC0).