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Dexmedetomidine

NDC 83634-600 · HUMAN PRESCRIPTION DRUG · INJECTION, SOLUTION, CONCENTRATE

Generic namedexmedetomidine
Labeler / ManufacturerAvenacy Inc.
Marketing categoryAbbreviated NDA (generic) · App ANDA209065
Dosage form / routeINJECTION, SOLUTION, CONCENTRATE · INTRAVENOUS
Active ingredientsDEXMEDETOMIDINE HYDROCHLORIDE (100 ug/mL)
Marketing started20240315
Package count1

External sources

Source: openFDA. Public-domain (CC0).