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Methylphenidate Hydrochloride

NDC 57664-607 · HUMAN PRESCRIPTION DRUG · TABLET, EXTENDED RELEASE

Labeler / ManufacturerSun Pharmaceutical Industries, Inc.
Marketing categoryAbbreviated NDA (generic) · App ANDA205135
Dosage form / routeTABLET, EXTENDED RELEASE · ORAL
Active ingredientsMETHYLPHENIDATE HYDROCHLORIDE (27 mg/1)
Marketing started20200820
Package count1

External sources

Source: openFDA. Public-domain (CC0).