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Labetalol Hydrochloride

NDC 0143-9623 · HUMAN PRESCRIPTION DRUG · INJECTION

Labeler / ManufacturerHikma Pharmaceuticals USA Inc.
Marketing categoryAbbreviated NDA (generic) · App ANDA075303
Dosage form / routeINJECTION · INTRAVENOUS
Active ingredientsLABETALOL HYDROCHLORIDE (5 mg/mL)
Marketing started19991129
Package count1

External sources

Source: openFDA. Public-domain (CC0).