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Dexmedetomidine Hydrochloride

NDC 42023-187 · HUMAN PRESCRIPTION DRUG · INJECTION, SOLUTION

Labeler / ManufacturerPar Health USA, LLC
Marketing categoryAbbreviated NDA (generic) · App ANDA208266
Dosage form / routeINJECTION, SOLUTION · INTRAVENOUS
Active ingredientsDEXMEDETOMIDINE HYDROCHLORIDE (4 ug/mL)
Marketing started20201204
Package count1

External sources

Source: openFDA. Public-domain (CC0).