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Labetalol Hydrochloride

NDC 67046-1697 · HUMAN PRESCRIPTION DRUG · TABLET

Labeler / ManufacturerCoupler LLC
Marketing categoryAbbreviated NDA (generic) · App ANDA074787
Dosage form / routeTABLET · ORAL
Active ingredientsLABETALOL HYDROCHLORIDE (200 mg/1)
Marketing started20261019
Package count1

External sources

Source: openFDA. Public-domain (CC0).