NDC 0409-4888 – Sodium Chloride

Sodium Chloride 9 mg/mL · Injection, Solution · Intramuscular, Intravenous, Subcutaneous

Human Prescription Drug 1 recall

Product NDC0409-4888

Product details

Brand name
Sodium Chloride
Generic name
Sodium Chloride
Labeler
Hospira, Inc.
Dosage form
Injection, Solution
Route
Intramuscular, Intravenous, Subcutaneous
Marketing category
NDA · NDA018803
Marketed since
February 28, 2005
Listing expires
December 31, 2026

Active ingredients

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

Package NDC codes (5)

Package NDCDescriptionSince
0409-4888-1025 VIAL, SINGLE-DOSE in 1 TRAY (0409-4888-10) / 10 mL in 1 VIAL, SINGLE-DOSE (0409-4888-02)Apr 30, 2005
0409-4888-1225 VIAL, SINGLE-DOSE in 1 TRAY (0409-4888-12) / 10 mL in 1 VIAL, SINGLE-DOSE (0409-4888-01)Jul 14, 2005
0409-4888-2025 VIAL, SINGLE-DOSE in 1 TRAY (0409-4888-20) / 20 mL in 1 VIAL, SINGLE-DOSE (0409-4888-03)Feb 28, 2005
0409-4888-5025 VIAL, SINGLE-DOSE in 1 TRAY (0409-4888-50) / 50 mL in 1 VIAL, SINGLE-DOSE (0409-4888-06)Feb 28, 2005
0409-4888-9010 VIAL, SINGLE-DOSE in 1 TRAY (0409-4888-90) / 10 mL in 1 VIAL, SINGLE-DOSE (0409-4888-02)Oct 20, 2021

Recalls mentioning this NDC

Other Sodium Chloride products