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Dexmedetomidine

NDC 55150-209 · HUMAN PRESCRIPTION DRUG · INJECTION, SOLUTION

Labeler / ManufacturerEugia US LLC
Marketing categoryAbbreviated NDA (generic) · App ANDA205867
Dosage form / routeINJECTION, SOLUTION · INTRAVENOUS
Active ingredientsDEXMEDETOMIDINE HYDROCHLORIDE (100 ug/mL)
Marketing started20160317
Package count1

External sources

Source: openFDA. Public-domain (CC0).