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propofol

NDC 16714-528 · HUMAN PRESCRIPTION DRUG · INJECTION, EMULSION

Labeler / ManufacturerNorthStar Rx LLC
Marketing categoryAbbreviated NDA (generic) · App ANDA206408
Dosage form / routeINJECTION, EMULSION · INTRAVENOUS
Active ingredientsPROPOFOL (10 mg/mL)
Marketing started20220701
Package count2

External sources

Source: openFDA. Public-domain (CC0).