Home > National Drug Code (NDC) > Sodium Chloride

Sodium Chloride - 0409-4888-50 - (Sodium Chloride)

Alphabetical Index


Drug Information of Sodium Chloride

Product NDC: 0409-4888
Proprietary Name: Sodium Chloride
Non Proprietary Name: Sodium Chloride
Active Ingredient(s): 9    mg/mL & nbsp;   Sodium Chloride
Administration Route(s): INTRAMUSCULAR; INTRAVENOUS; SUBCUTANEOUS
Dosage Form(s): INJECTION, SOLUTION
Coding System: National Drug Codes(NDC)

Labeler Information of Sodium Chloride

Product NDC: 0409-4888
Labeler Name: Hospira, Inc.
Product Type: HUMAN PRESCRIPTION DRUG
FDA Application Number: NDA018803
Marketing Category: NDA
Start Marketing Date: 20110908

Package Information of Sodium Chloride

Package NDC: 0409-4888-50
Package Description: 25 VIAL, SINGLE-DOSE in 1 TRAY (0409-4888-50) > 50 mL in 1 VIAL, SINGLE-DOSE

NDC Information of Sodium Chloride

NDC Code 0409-4888-50
Proprietary Name Sodium Chloride
Package Description 25 VIAL, SINGLE-DOSE in 1 TRAY (0409-4888-50) > 50 mL in 1 VIAL, SINGLE-DOSE
Product NDC 0409-4888
Product Type Name HUMAN PRESCRIPTION DRUG
Non Proprietary Name Sodium Chloride
Dosage Form Name INJECTION, SOLUTION
Route Name INTRAMUSCULAR; INTRAVENOUS; SUBCUTANEOUS
Start Marketing Date 20110908
Marketing Category Name NDA
Labeler Name Hospira, Inc.
Substance Name SODIUM CHLORIDE
Strength Number 9
Strength Unit mg/mL
Pharmaceutical Classes

Complete Information of Sodium Chloride


General Information