FDA NDC Directory · JSON-LD · Markdown

METHYLPHENIDATE HYDROCHLORIDE

NDC 50268-529 · HUMAN PRESCRIPTION DRUG · TABLET

Labeler / ManufacturerAvPAK
Marketing categoryAbbreviated NDA (generic) · App ANDA207416
Dosage form / routeTABLET · ORAL
Active ingredientsMETHYLPHENIDATE HYDROCHLORIDE (20 mg/1)
Marketing started20200213
Package count1

External sources

Source: openFDA. Public-domain (CC0).