FDA NDC Directory · JSON-LD · Markdown

Methylphenidate Hydrochloride

NDC 50268-548 · HUMAN PRESCRIPTION DRUG · TABLET, EXTENDED RELEASE

Labeler / ManufacturerAvPAK
Marketing categoryAbbreviated NDA (generic) · App ANDA211009
Dosage form / routeTABLET, EXTENDED RELEASE · ORAL
Active ingredientsMETHYLPHENIDATE HYDROCHLORIDE (54 mg/1)
Marketing started20210422
Package count1

External sources

Source: openFDA. Public-domain (CC0).