FDA NDC Directory · JSON-LD · Markdown

Methylphenidate Hydrochloride

NDC 10702-101 · HUMAN PRESCRIPTION DRUG · TABLET

Labeler / ManufacturerKVK-TECH, INC.
Marketing categoryAbbreviated NDA (generic) · App ANDA206932
Dosage form / routeTABLET · ORAL
Active ingredientsMETHYLPHENIDATE HYDROCHLORIDE (10 mg/1)
Marketing started20170511
Package count1

External sources

Source: openFDA. Public-domain (CC0).