FDA NDC Directory · JSON-LD · Markdown

propofol

NDC 71288-730 · HUMAN PRESCRIPTION DRUG · INJECTION, EMULSION

Labeler / ManufacturerMeitheal Pharmaceuticals Inc.
Marketing categoryAbbreviated NDA (generic) · App ANDA217945
Dosage form / routeINJECTION, EMULSION · INTRAVENOUS
Active ingredientsPROPOFOL (10 mg/mL)
Marketing started20251202
Package count1

External sources

Source: openFDA. Public-domain (CC0).