Home > National Drug Code (NDC) > Sodium Chloride

Sodium Chloride - 0409-1966-14 - (SODIUM CHLORIDE)

Alphabetical Index


Drug Information of Sodium Chloride

Product NDC: 0409-1966
Proprietary Name: Sodium Chloride
Non Proprietary Name: SODIUM CHLORIDE
Active Ingredient(s): 9    mg/mL & nbsp;   SODIUM CHLORIDE
Administration Route(s): INTRAVENOUS
Dosage Form(s): INJECTION
Coding System: National Drug Codes(NDC)

Labeler Information of Sodium Chloride

Product NDC: 0409-1966
Labeler Name: Hospira, Inc.
Product Type: HUMAN PRESCRIPTION DRUG
FDA Application Number: NDA018800
Marketing Category: NDA
Start Marketing Date: 20110819

Package Information of Sodium Chloride

Package NDC: 0409-1966-14
Package Description: 25 VIAL, MULTI-DOSE in 1 CARTON (0409-1966-14) > 30 mL in 1 VIAL, MULTI-DOSE

NDC Information of Sodium Chloride

NDC Code 0409-1966-14
Proprietary Name Sodium Chloride
Package Description 25 VIAL, MULTI-DOSE in 1 CARTON (0409-1966-14) > 30 mL in 1 VIAL, MULTI-DOSE
Product NDC 0409-1966
Product Type Name HUMAN PRESCRIPTION DRUG
Non Proprietary Name SODIUM CHLORIDE
Dosage Form Name INJECTION
Route Name INTRAVENOUS
Start Marketing Date 20110819
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