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Dexmedetomidine Hydrochloride

NDC 57664-596 · HUMAN PRESCRIPTION DRUG · INJECTION, SOLUTION

Generic nameDEXMEDETOMIDINE HYDROCHLORIDE
Labeler / ManufacturerSun Pharmaceuticals Industries, Inc.
Marketing categoryAbbreviated NDA (generic) · App ANDA202126
Dosage form / routeINJECTION, SOLUTION · INTRAVENOUS
Active ingredientsDEXMEDETOMIDINE HYDROCHLORIDE (100 ug/mL)
Marketing started20150408
Package count1

External sources

Source: openFDA. Public-domain (CC0).