NDC 0409-4699 – Propofol

Propofol 10 mg/mL · Injection, Emulsion · Intravenous

Human Prescription Drug 10 recalls

Product NDC0409-4699

Product details

Brand name
Propofol
Generic name
Propofol
Labeler
Hospira, Inc.
Dosage form
Injection, Emulsion
Route
Intravenous
Marketing category
ANDA · ANDA077908
Marketed since
April 3, 2006
Listing expires
December 31, 2027
Pharmacologic class
General Anesthetic

Active ingredients

Uses, dosage, side effects and warnings for Propofol →

Package NDC codes (2)

Package NDCDescriptionSince
0409-4699-2410 VIAL in 1 TRAY (0409-4699-24) / 100 mL in 1 VIAL (0409-4699-54)Apr 3, 2006
0409-4699-3320 VIAL in 1 TRAY (0409-4699-33) / 50 mL in 1 VIAL (0409-4699-53)Apr 3, 2006

Recalls mentioning this NDC

Other Propofol products