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Labetalol hydrochloride

NDC 0591-0606 · HUMAN PRESCRIPTION DRUG · TABLET, FILM COATED

Labeler / ManufacturerActavis Pharma, Inc.
Marketing categoryAbbreviated NDA (generic) · App ANDA075133
Dosage form / routeTABLET, FILM COATED · ORAL
Active ingredientsLABETALOL HYDROCHLORIDE (200 mg/1)
Marketing started19980803
Marketing ended20260630
Package count1

External sources

Source: openFDA. Public-domain (CC0).