FDA NDC Directory · JSON-LD · Markdown

Betaxolol

NDC 24658-701 · HUMAN PRESCRIPTION DRUG · TABLET, FILM COATED

Labeler / ManufacturerPuraCap Laboratories LLC
Marketing categoryAbbreviated NDA (generic) · App ANDA075541
Dosage form / routeTABLET, FILM COATED · ORAL
Active ingredientsBETAXOLOL HYDROCHLORIDE (20 mg/1)
Marketing started20160822
Package count1

External sources

Source: openFDA. Public-domain (CC0).