NDC 0409-7299 – Sodium Acetate

Sodium Acetate Anhydrous 3.28 g/20mL · Injection, Solution, Concentrate · Intravenous

Human Prescription Drug 1 recall

Product NDC0409-7299

Product details

Brand name
Sodium Acetate
Generic name
Sodium Acetate
Labeler
Hospira, Inc.
Dosage form
Injection, Solution, Concentrate
Route
Intravenous
Marketing category
NDA · NDA018893
Marketed since
March 5, 2014
Listing expires
December 31, 2027
Pharmacologic class
Osmotic Laxative

Active ingredients

Uses, dosage, side effects and warnings for Sodium Acetate →

Package NDC codes (2)

Package NDCDescriptionSince
0409-7299-2525 VIAL, SINGLE-DOSE in 1 TRAY (0409-7299-25) / 20 mL in 1 VIAL, SINGLE-DOSE (0409-7299-45)Mar 5, 2014
0409-7299-7325 VIAL, SINGLE-DOSE in 1 TRAY (0409-7299-73) / 20 mL in 1 VIAL, SINGLE-DOSE (0409-7299-83)Mar 31, 2005

Recalls mentioning this NDC

Other Sodium Acetate products