FDA NDC Directory · JSON-LD · Markdown

Methylphenidate Hydrochloride

NDC 13107-380 · HUMAN PRESCRIPTION DRUG · TABLET

Labeler / ManufacturerAurolife Pharma, LLC
Marketing categoryAbbreviated NDA (generic) · App ANDA209276
Dosage form / routeTABLET · ORAL
Active ingredientsMETHYLPHENIDATE HYDROCHLORIDE (5 mg/1)
Marketing started20170411
Package count1

External sources

Source: openFDA. Public-domain (CC0).