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Labetalol Hydrochloride

NDC 68001-701 · HUMAN PRESCRIPTION DRUG · TABLET

Labeler / ManufacturerBluePoint Laboratories
Marketing categoryAbbreviated NDA (generic) · App ANDA074787
Dosage form / routeTABLET · ORAL
Active ingredientsLABETALOL HYDROCHLORIDE (200 mg/1)
Marketing started20260315
Package count2

External sources

Source: openFDA. Public-domain (CC0).