FDA NDC Directory · JSON-LD · Markdown

BETAXOLOL HYDROCHLORIDE

NDC 10702-014 · HUMAN PRESCRIPTION DRUG · TABLET, COATED

Generic namebetaxolol hydrochloride
Labeler / ManufacturerKVK-TECH, INC.
Marketing categoryAbbreviated NDA (generic) · App ANDA078962
Dosage form / routeTABLET, COATED · ORAL
Active ingredientsBETAXOLOL HYDROCHLORIDE (20 mg/1)
Marketing started20111102
Package count1

External sources

Source: openFDA. Public-domain (CC0).