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Dextrose and Sodium Chloride - 0338-0095-03 - (Dextrose and Sodium Chloride)

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Drug Information of Dextrose and Sodium Chloride

Product NDC: 0338-0095
Proprietary Name: Dextrose and Sodium Chloride
Non Proprietary Name: Dextrose and Sodium Chloride
Active Ingredient(s): 10; 900    g/100mL; mg/100mL & nbsp;   Dextrose and Sodium Chloride
Administration Route(s): INTRAVENOUS
Dosage Form(s): INJECTION, SOLUTION
Coding System: National Drug Codes(NDC)

Labeler Information of Dextrose and Sodium Chloride

Product NDC: 0338-0095
Labeler Name: Baxter Healthcare Corporation
Product Type: HUMAN PRESCRIPTION DRUG
FDA Application Number: NDA016696
Marketing Category: NDA
Start Marketing Date: 19710322

Package Information of Dextrose and Sodium Chloride

Package NDC: 0338-0095-03
Package Description: 500 mL in 1 BAG (0338-0095-03)

NDC Information of Dextrose and Sodium Chloride

NDC Code 0338-0095-03
Proprietary Name Dextrose and Sodium Chloride
Package Description 500 mL in 1 BAG (0338-0095-03)
Product NDC 0338-0095
Product Type Name HUMAN PRESCRIPTION DRUG
Non Proprietary Name Dextrose and Sodium Chloride
Dosage Form Name INJECTION, SOLUTION
Route Name INTRAVENOUS
Start Marketing Date 19710322
Marketing Category Name NDA
Labeler Name Baxter Healthcare Corporation
Substance Name DEXTROSE MONOHYDRATE; SODIUM CHLORIDE
Strength Number 10; 900
Strength Unit g/100mL; mg/100mL
Pharmaceutical Classes

Complete Information of Dextrose and Sodium Chloride


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