FDA NDC Directory · JSON-LD · Markdown

LABETALOL HYDROCHLORIDE

NDC 67296-2156 · HUMAN PRESCRIPTION DRUG · TABLET, FILM COATED

Generic nameLabetalol Hydrochloride
Labeler / ManufacturerRedpharm Drug
Marketing categoryAbbreviated NDA (generic) · App ANDA211953
Dosage form / routeTABLET, FILM COATED · ORAL
Active ingredientsLABETALOL HYDROCHLORIDE (100 mg/1)
Marketing started20210818
Package count1

External sources

Source: openFDA. Public-domain (CC0).