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Sodium Chloride - 0338-0049-48 - (Sodium Chloride)

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Drug Information of Sodium Chloride

Product NDC: 0338-0049
Proprietary Name: Sodium Chloride
Non Proprietary Name: Sodium Chloride
Active Ingredient(s): 9    g/1000mL & 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: 0338-0049
Labeler Name: Baxter Healthcare Corporation
Product Type: HUMAN PRESCRIPTION DRUG
FDA Application Number: NDA016677
Marketing Category: NDA
Start Marketing Date: 19701209

Package Information of Sodium Chloride

Package NDC: 0338-0049-48
Package Description: 1 BAG in 1 PACKAGE (0338-0049-48) > 100 mL in 1 BAG

NDC Information of Sodium Chloride

NDC Code 0338-0049-48
Proprietary Name Sodium Chloride
Package Description 1 BAG in 1 PACKAGE (0338-0049-48) > 100 mL in 1 BAG
Product NDC 0338-0049
Product Type Name HUMAN PRESCRIPTION DRUG
Non Proprietary Name Sodium Chloride
Dosage Form Name INJECTION, SOLUTION
Route Name INTRAVENOUS
Start Marketing Date 19701209
Marketing Category Name NDA
Labeler Name Baxter Healthcare Corporation
Substance Name SODIUM CHLORIDE
Strength Number 9
Strength Unit g/1000mL
Pharmaceutical Classes

Complete Information of Sodium Chloride


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