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LABETALOL HYDROCHLORIDE

NDC 70518-3499 · HUMAN PRESCRIPTION DRUG · TABLET, FILM COATED

Generic nameLabetalol Hydrochloride
Labeler / ManufacturerREMEDYREPACK INC.
Marketing categoryAbbreviated NDA (generic) · App ANDA211953
Dosage form / routeTABLET, FILM COATED · ORAL
Active ingredientsLABETALOL HYDROCHLORIDE (100 mg/1)
Marketing started20220825
Package count3

External sources

Source: openFDA. Public-domain (CC0).