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Labetalol Hydrochloride

NDC 72603-902 · HUMAN PRESCRIPTION DRUG · TABLET

Labeler / ManufacturerNorthStar Rx LLC
Marketing categoryAbbreviated NDA (generic) · App ANDA074787
Dosage form / routeTABLET · ORAL
Active ingredientsLABETALOL HYDROCHLORIDE (100 mg/1)
Marketing started20260319
Package count2

External sources

Source: openFDA. Public-domain (CC0).