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Labetalol Hydrochloride

NDC 68001-381 · HUMAN PRESCRIPTION DRUG · TABLET, FILM COATED

Labeler / ManufacturerBluePoint Laboratories Inc.
Marketing categoryAbbreviated NDA (generic) · App ANDA207743
Dosage form / routeTABLET, FILM COATED · ORAL
Active ingredientsLABETALOL HYDROCHLORIDE (100 mg/1)
Marketing started20190218
Package count2

External sources

Source: openFDA. Public-domain (CC0).