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Sodium Chloride - 0338-0553-11 - (Sodium Chloride)

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Drug Information of Sodium Chloride

Product NDC: 0338-0553
Proprietary Name: Sodium Chloride
Non Proprietary Name: Sodium Chloride
Active Ingredient(s): 900    mg/100mL & nbsp;   Sodium Chloride
Administration Route(s): INTRAVENOUS
Dosage Form(s): INJECTION
Coding System: National Drug Codes(NDC)

Labeler Information of Sodium Chloride

Product NDC: 0338-0553
Labeler Name: Baxter Healthcare Corporation
Product Type: HUMAN PRESCRIPTION DRUG
FDA Application Number: ANDA020178
Marketing Category: ANDA
Start Marketing Date: 19921207

Package Information of Sodium Chloride

Package NDC: 0338-0553-11
Package Description: 50 mL in 1 BAG (0338-0553-11)

NDC Information of Sodium Chloride

NDC Code 0338-0553-11
Proprietary Name Sodium Chloride
Package Description 50 mL in 1 BAG (0338-0553-11)
Product NDC 0338-0553
Product Type Name HUMAN PRESCRIPTION DRUG
Non Proprietary Name Sodium Chloride
Dosage Form Name INJECTION
Route Name INTRAVENOUS
Start Marketing Date 19921207
Marketing Category Name ANDA
Labeler Name Baxter Healthcare Corporation
Substance Name SODIUM CHLORIDE
Strength Number 900
Strength Unit mg/100mL
Pharmaceutical Classes

Complete Information of Sodium Chloride


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