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DEXMEDETOMIDINE HYDROCHLORIDE IN 0.9% SODIUM CHLORIDE

NDC 0781-3493 · HUMAN PRESCRIPTION DRUG · INJECTION

Labeler / ManufacturerSandoz Inc.
Marketing categoryAbbreviated NDA (generic) · App ANDA209065
Dosage form / routeINJECTION · INTRAVENOUS
Active ingredientsDEXMEDETOMIDINE HYDROCHLORIDE (4 ug/mL)
Marketing started20200612
Package count1

External sources

Source: openFDA. Public-domain (CC0).