FDA NDC Directory · JSON-LD · Markdown

Labetalol hydrochloride

NDC 0591-0605 · 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 (100 mg/1)
Marketing started19980803
Marketing ended20260930
Package count2

External sources

Source: openFDA. Public-domain (CC0).