NDC 0409-7101 – Sodium Chloride

Sodium Chloride 900 mg/100mL · Injection, Solution · Intravenous

Human Prescription Drug 2 recalls

Product NDC0409-7101

Product details

Brand name
Sodium Chloride
Generic name
Sodium Chloride
Labeler
Hospira, Inc.
Dosage form
Injection, Solution
Route
Intravenous
Marketing category
NDA · NDA019465
Marketed since
June 30, 2005
Marketing end
December 31, 2026
Pharmacologic class
Osmotic Laxative

Active ingredients

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

Package NDC codes (2)

Package NDCDescriptionSince
0409-7101-0224 POUCH in 1 CASE (0409-7101-02) / 1 BAG in 1 POUCH / 250 mL in 1 BAG (0409-7101-04)Jun 30, 2005
0409-7101-6710 POUCH in 1 CASE (0409-7101-67) / 5 BAG in 1 POUCH / 100 mL in 1 BAG (0409-7101-69)Aug 24, 2005

Recalls mentioning this NDC

Other Sodium Chloride products