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Sodium Chloride - 0409-1141-02 - (SODIUM CHLORIDE)

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Drug Information of Sodium Chloride

Product NDC: 0409-1141
Proprietary Name: Sodium Chloride
Non Proprietary Name: SODIUM CHLORIDE
Active Ingredient(s): 234    mg/mL & nbsp;   SODIUM CHLORIDE
Administration Route(s): INTRAVENOUS
Dosage Form(s): INJECTION, SOLUTION
Coding System: National Drug Codes(NDC)

Labeler Information of Sodium Chloride

Product NDC: 0409-1141
Labeler Name: Hospira, Inc.
Product Type: HUMAN PRESCRIPTION DRUG
FDA Application Number:
Marketing Category: UNAPPROVED DRUG OTHER
Start Marketing Date: 20050430

Package Information of Sodium Chloride

Package NDC: 0409-1141-02
Package Description: 25 VIAL in 1 CASE (0409-1141-02) > 100 mL in 1 VIAL

NDC Information of Sodium Chloride

NDC Code 0409-1141-02
Proprietary Name Sodium Chloride
Package Description 25 VIAL in 1 CASE (0409-1141-02) > 100 mL in 1 VIAL
Product NDC 0409-1141
Product Type Name HUMAN PRESCRIPTION DRUG
Non Proprietary Name SODIUM CHLORIDE
Dosage Form Name INJECTION, SOLUTION
Route Name INTRAVENOUS
Start Marketing Date 20050430
Marketing Category Name UNAPPROVED DRUG OTHER
Labeler Name Hospira, Inc.
Substance Name SODIUM CHLORIDE
Strength Number 234
Strength Unit mg/mL
Pharmaceutical Classes

Complete Information of Sodium Chloride


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