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DEXMEDETOMIDINE

NDC 71288-505 · HUMAN PRESCRIPTION DRUG · INJECTION, SOLUTION

Labeler / ManufacturerMeitheal Pharmaceuticals Inc.
Marketing categoryAbbreviated NDA (generic) · App ANDA204843
Dosage form / routeINJECTION, SOLUTION · INTRAVENOUS
Active ingredientsDEXMEDETOMIDINE HYDROCHLORIDE (100 ug/mL)
Marketing started20190118
Package count1

External sources

Source: openFDA. Public-domain (CC0).