NDC 0409-6010 – Propofol

Propofol 10 mg/mL · Injection, Emulsion · Intravenous

Human Prescription Drug 10 recalls

Product NDC0409-6010

Product details

Brand name
Propofol
Generic name
Propofol
Labeler
Hospira, Inc.
Dosage form
Injection, Emulsion
Route
Intravenous
Marketing category
ANDA · ANDA077908
Marketed since
May 22, 2022
Listing expires
December 31, 2027
Pharmacologic class
General Anesthetic

Active ingredients

Uses, dosage, side effects and warnings for Propofol →

Package NDC codes (1)

Package NDCDescriptionSince
0409-6010-2525 VIAL in 1 TRAY (0409-6010-25) / 20 mL in 1 VIAL (0409-6010-02)May 22, 2022

Recalls mentioning this NDC

Other Propofol products