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Sodium Chloride - 0409-7138-36 - (SODIUM CHLORIDE)

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Drug Information of Sodium Chloride

Product NDC: 0409-7138
Proprietary Name: Sodium Chloride
Non Proprietary Name: SODIUM CHLORIDE
Active Ingredient(s): 900    mg/100mL & nbsp;   SODIUM CHLORIDE
Administration Route(s): IRRIGATION
Dosage Form(s): IRRIGANT
Coding System: National Drug Codes(NDC)

Labeler Information of Sodium Chloride

Product NDC: 0409-7138
Labeler Name: Hospira, Inc.
Product Type: HUMAN PRESCRIPTION DRUG
FDA Application Number: NDA017514
Marketing Category: NDA
Start Marketing Date: 20100517

Package Information of Sodium Chloride

Package NDC: 0409-7138-36
Package Description: 9 BOTTLE, PLASTIC in 1 CASE (0409-7138-36) > 1500 mL in 1 BOTTLE, PLASTIC

NDC Information of Sodium Chloride

NDC Code 0409-7138-36
Proprietary Name Sodium Chloride
Package Description 9 BOTTLE, PLASTIC in 1 CASE (0409-7138-36) > 1500 mL in 1 BOTTLE, PLASTIC
Product NDC 0409-7138
Product Type Name HUMAN PRESCRIPTION DRUG
Non Proprietary Name SODIUM CHLORIDE
Dosage Form Name IRRIGANT
Route Name IRRIGATION
Start Marketing Date 20100517
Marketing Category Name NDA
Labeler Name Hospira, Inc.
Substance Name SODIUM CHLORIDE
Strength Number 900
Strength Unit mg/100mL
Pharmaceutical Classes

Complete Information of Sodium Chloride


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