FDA NDC Directory · JSON-LD · Markdown

Dexmethylphenidate Hydrochloride

NDC 10702-108 · HUMAN PRESCRIPTION DRUG · TABLET

Labeler / ManufacturerKVK-TECH, INC
Marketing categoryAbbreviated NDA (generic) · App ANDA206931
Dosage form / routeTABLET · ORAL
Active ingredientsDEXMETHYLPHENIDATE HYDROCHLORIDE (10 mg/1)
Marketing started20151204
Package count1

External sources

Source: openFDA. Public-domain (CC0).