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LABETALOL HYDROCHLORIDE

NDC 72888-468 · HUMAN PRESCRIPTION DRUG · TABLET, FILM COATED

Generic nameLabetalol Hydrochloride
Labeler / ManufacturerAdvagen Pharma Ltd
Marketing categoryAbbreviated NDA (generic) · App ANDA211953
Dosage form / routeTABLET, FILM COATED · ORAL
Active ingredientsLABETALOL HYDROCHLORIDE (300 mg/1)
Marketing started20250520
Package count2

External sources

Source: openFDA. Public-domain (CC0).