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Esmolol Hydrochloride

NDC 68083-211 · HUMAN PRESCRIPTION DRUG · INJECTION

Labeler / ManufacturerGland Pharma Limited
Marketing categoryAbbreviated NDA (generic) · App ANDA208538
Dosage form / routeINJECTION · INTRAVENOUS
Active ingredientsESMOLOL HYDROCHLORIDE (10 mg/mL)
Marketing started20190819
Package count1

External sources

Source: openFDA. Public-domain (CC0).