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Labetalol Hydrochloride

NDC 70377-061 · HUMAN PRESCRIPTION DRUG · TABLET, FILM COATED

Labeler / ManufacturerBiocon Pharma Inc.
Marketing categoryAbbreviated NDA (generic) · App ANDA209603
Dosage form / routeTABLET, FILM COATED · ORAL
Active ingredientsLABETALOL HYDROCHLORIDE (200 mg/1)
Marketing started20210527
Package count3

External sources

Source: openFDA. Public-domain (CC0).