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Dexmedetomidine Hydrochloride

NDC 63323-671 · HUMAN PRESCRIPTION DRUG · INJECTION, SOLUTION

Labeler / ManufacturerFresenius Kabi USA, LLC
Marketing categoryAbbreviated NDA (generic) · App ANDA208129
Dosage form / routeINJECTION, SOLUTION · INTRAVENOUS
Active ingredientsDEXMEDETOMIDINE HYDROCHLORIDE (4 ug/mL)
Marketing started20190513
Package count3

External sources

Source: openFDA. Public-domain (CC0).