FDA NDC Directory · JSON-LD · Markdown

PROPOFOL

NDC 83854-018 · HUMAN PRESCRIPTION DRUG · INJECTION, EMULSION

Labeler / ManufacturerAnthea Pharma Private Limited
Marketing categoryAbbreviated NDA (generic) · App ANDA220857
Dosage form / routeINJECTION, EMULSION · INTRAVENOUS
Active ingredientsPROPOFOL (10 mg/mL)
Marketing started20260714
Package count4

External sources

Source: openFDA. Public-domain (CC0).