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Labetalol Hydrochloride

NDC 58657-604 · HUMAN PRESCRIPTION DRUG · TABLET, FILM COATED

Labeler / ManufacturerMethod Pharmaceuticals, LLC
Marketing categoryAbbreviated NDA (generic) · App ANDA075215
Dosage form / routeTABLET, FILM COATED · ORAL
Active ingredientsLABETALOL (300 mg/1)
Marketing started20191122
Package count2

External sources

Source: openFDA. Public-domain (CC0).