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Dexmedetomidine Hydrochloride

NDC 65219-642 · HUMAN PRESCRIPTION DRUG · INJECTION, SOLUTION

Generic namedexmedetomidine hydrochloride
Labeler / ManufacturerFresenius Kabi USA, LLC
Marketing categoryAbbreviated NDA (generic) · App ANDA201072
Dosage form / routeINJECTION, SOLUTION · INTRAVENOUS
Active ingredientsDEXMEDETOMIDINE HYDROCHLORIDE (100 ug/mL)
Marketing started20150918
Package count1

External sources

Source: openFDA. Public-domain (CC0).