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Dextrose and Sodium Chloride - 0409-7925-48 - (DEXTROSE MONOHYDRATE and SODIUM CHLORIDE)

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Drug Information of Dextrose and Sodium Chloride

Product NDC: 0409-7925
Proprietary Name: Dextrose and Sodium Chloride
Non Proprietary Name: DEXTROSE MONOHYDRATE and SODIUM CHLORIDE
Active Ingredient(s): 5; .3    g/100mL; g/100mL & nbsp;   DEXTROSE MONOHYDRATE 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: 0409-7925
Labeler Name: Hospira, Inc.
Product Type: HUMAN PRESCRIPTION DRUG
FDA Application Number: NDA017799
Marketing Category: NDA
Start Marketing Date: 20110215

Package Information of Dextrose and Sodium Chloride

Package NDC: 0409-7925-48
Package Description: 12 BAG in 1 CASE (0409-7925-48) > 1000 mL in 1 BAG

NDC Information of Dextrose and Sodium Chloride

NDC Code 0409-7925-48
Proprietary Name Dextrose and Sodium Chloride
Package Description 12 BAG in 1 CASE (0409-7925-48) > 1000 mL in 1 BAG
Product NDC 0409-7925
Product Type Name HUMAN PRESCRIPTION DRUG
Non Proprietary Name DEXTROSE MONOHYDRATE and SODIUM CHLORIDE
Dosage Form Name INJECTION, SOLUTION
Route Name INTRAVENOUS
Start Marketing Date 20110215
Marketing Category Name NDA
Labeler Name Hospira, Inc.
Substance Name DEXTROSE MONOHYDRATE; SODIUM CHLORIDE
Strength Number 5; .3
Strength Unit g/100mL; g/100mL
Pharmaceutical Classes

Complete Information of Dextrose and Sodium Chloride


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