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Heparin Sodium - 0409-7620-03 - (HEPARIN SODIUM)

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Drug Information of Heparin Sodium

Product NDC: 0409-7620
Proprietary Name: Heparin Sodium
Non Proprietary Name: HEPARIN SODIUM
Active Ingredient(s): 200    [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

Product NDC: 0409-7620
Labeler Name: Hospira, Inc.
Product Type: HUMAN PRESCRIPTION DRUG
FDA Application Number: NDA018916
Marketing Category: NDA
Start Marketing Date: 20050331

Package Information of Heparin Sodium

Package NDC: 0409-7620-03
Package Description: 18 POUCH in 1 CASE (0409-7620-03) > 1 BAG in 1 POUCH > 500 mL in 1 BAG

NDC Information of Heparin Sodium

NDC Code 0409-7620-03
Proprietary Name Heparin Sodium
Package Description 18 POUCH in 1 CASE (0409-7620-03) > 1 BAG in 1 POUCH > 500 mL in 1 BAG
Product NDC 0409-7620
Product Type Name HUMAN PRESCRIPTION DRUG
Non Proprietary Name HEPARIN SODIUM
Dosage Form Name INJECTION, SOLUTION
Route Name INTRAVENOUS
Start Marketing Date 20050331
Marketing Category Name NDA
Labeler Name Hospira, Inc.
Substance Name HEPARIN SODIUM
Strength Number 200
Strength Unit [USP'U]/100mL
Pharmaceutical Classes Anti-coagulant [EPC],Heparin [Chemical/Ingredient],Unfractionated Heparin [EPC]

Complete Information of Heparin Sodium


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