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Dextrose and Sodium Chloride - 0409-7941-03 - (DEXTROSE MONOHYDRATE and SODIUM CHLORIDE)

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Drug Information of Dextrose and Sodium Chloride

Product NDC: 0409-7941
Proprietary Name: Dextrose and Sodium Chloride
Non Proprietary Name: DEXTROSE MONOHYDRATE and SODIUM CHLORIDE
Active Ingredient(s): 5; .9    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: 0409-7941
Labeler Name: Hospira, Inc.
Product Type: HUMAN PRESCRIPTION DRUG
FDA Application Number: ANDA017585
Marketing Category: ANDA
Start Marketing Date: 20110216

Package Information of Dextrose and Sodium Chloride

Package NDC: 0409-7941-03
Package Description: 24 POUCH in 1 CASE (0409-7941-03) > 1 BAG in 1 POUCH > 500 mL in 1 BAG

NDC Information of Dextrose and Sodium Chloride

NDC Code 0409-7941-03
Proprietary Name Dextrose and Sodium Chloride
Package Description 24 POUCH in 1 CASE (0409-7941-03) > 1 BAG in 1 POUCH > 500 mL in 1 BAG
Product NDC 0409-7941
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 20110216
Marketing Category Name ANDA
Labeler Name Hospira, Inc.
Substance Name DEXTROSE MONOHYDRATE; SODIUM CHLORIDE
Strength Number 5; .9
Strength Unit g/100mL; g/100mL
Pharmaceutical Classes

Complete Information of Dextrose and Sodium Chloride


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