FDA NDC Directory · JSON-LD · Markdown

PROPOFOL

NDC 0409-0501 · HUMAN PRESCRIPTION DRUG · INJECTION, EMULSION

Labeler / ManufacturerHospira, Inc.
Marketing categoryAbbreviated NDA (generic) · App ANDA077908
Dosage form / routeINJECTION, EMULSION · INTRAVENOUS
Active ingredientsPROPOFOL (10 mg/mL)
Marketing started20260817
Package count1

External sources

Source: openFDA. Public-domain (CC0).