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propofol

NDC 23155-345 · HUMAN PRESCRIPTION DRUG · INJECTION, EMULSION

Labeler / ManufacturerHeritage Pharmaceuticals Inc. d/b/a Avet Pharmaceuticals Inc.
Marketing categoryAbbreviated NDA (generic) · App ANDA206408
Dosage form / routeINJECTION, EMULSION · INTRAVENOUS
Active ingredientsPROPOFOL (10 mg/mL)
Marketing started20211012
Package count4

External sources

Source: openFDA. Public-domain (CC0).