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Heparin Sodium and Dextrose - 0409-7793-23 - (HEPARIN SODIUM)

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Drug Information of Heparin Sodium and Dextrose

Product NDC: 0409-7793
Proprietary Name: Heparin Sodium and Dextrose
Non Proprietary Name: HEPARIN SODIUM
Active Ingredient(s): 10000    [USP'U]/100mL & nbsp;   HEPARIN SODIUM
Administration Route(s): INTRAVENOUS
Dosage Form(s): INJECTION, SOLUTION
Coding System: National Drug Codes(NDC)

Labeler Information of Heparin Sodium and Dextrose

Product NDC: 0409-7793
Labeler Name: Hospira, Inc.
Product Type: HUMAN PRESCRIPTION DRUG
FDA Application Number: NDA019339
Marketing Category: NDA
Start Marketing Date: 19850327

Package Information of Heparin Sodium and Dextrose

Package NDC: 0409-7793-23
Package Description: 24 POUCH in 1 CASE (0409-7793-23) > 1 BAG in 1 POUCH > 100 mL in 1 BAG

NDC Information of Heparin Sodium and Dextrose

NDC Code 0409-7793-23
Proprietary Name Heparin Sodium and Dextrose
Package Description 24 POUCH in 1 CASE (0409-7793-23) > 1 BAG in 1 POUCH > 100 mL in 1 BAG
Product NDC 0409-7793
Product Type Name HUMAN PRESCRIPTION DRUG
Non Proprietary Name HEPARIN SODIUM
Dosage Form Name INJECTION, SOLUTION
Route Name INTRAVENOUS
Start Marketing Date 19850327
Marketing Category Name NDA
Labeler Name Hospira, Inc.
Substance Name HEPARIN SODIUM
Strength Number 10000
Strength Unit [USP'U]/100mL
Pharmaceutical Classes Anti-coagulant [EPC],Heparin [Chemical/Ingredient],Unfractionated Heparin [EPC]

Complete Information of Heparin Sodium and Dextrose


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