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Labetalol Hydrochloride

NDC 68083-111 · HUMAN PRESCRIPTION DRUG · INJECTION, SOLUTION

Labeler / ManufacturerGland Pharma Limited
Marketing categoryAbbreviated NDA (generic) · App ANDA090699
Dosage form / routeINJECTION, SOLUTION · INTRAVENOUS
Active ingredientsLABETALOL HYDROCHLORIDE (5 mg/mL)
Marketing started20120419
Package count2

External sources

Source: openFDA. Public-domain (CC0).