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DEXMEDETOMIDINE HYDROCHLORIDE

NDC 67457-924 · HUMAN PRESCRIPTION DRUG · INJECTION, SOLUTION

Labeler / ManufacturerMylan Institutional LLC
Marketing categoryAbbreviated NDA (generic) · App ANDA212571
Dosage form / routeINJECTION, SOLUTION · INTRAVENOUS
Active ingredientsDEXMEDETOMIDINE HYDROCHLORIDE (200 ug/50mL)
Marketing started20201113
Package count1

External sources

Source: openFDA. Public-domain (CC0).