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DEXMEDETOMIDINE HYDROCHLORIDE

NDC 71225-133 · HUMAN PRESCRIPTION DRUG · INJECTION

Generic namedexmedetomidine hydrochloride
Labeler / ManufacturerSlayback Pharma LLC
Marketing categoryAbbreviated NDA (generic) · App ANDA212791
Dosage form / routeINJECTION · INTRAVENOUS
Active ingredientsDEXMEDETOMIDINE HYDROCHLORIDE (4 ug/mL)
Marketing started20211020
Package count1

External sources

Source: openFDA. Public-domain (CC0).