FDA NDC Directory · JSON-LD · Markdown

PROPOFOL

NDC 51662-1471 · HUMAN PRESCRIPTION DRUG · INJECTION, EMULSION

Labeler / ManufacturerHF Acquisition Co LLC, DBA HealthFirst
Marketing categoryAbbreviated NDA (generic) · App ANDA077908
Dosage form / routeINJECTION, EMULSION · INTRAVENOUS
Active ingredientsPROPOFOL (10 mg/mL)
Marketing started20191215
Package count1

External sources

Source: openFDA. Public-domain (CC0).