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Heparin Sodium - 0409-2581-02 - (HEPARIN SODIUM)

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Drug Information of Heparin Sodium

Product NDC: 0409-2581
Proprietary Name: Heparin Sodium
Non Proprietary Name: HEPARIN SODIUM
Active Ingredient(s): 10000    [USP'U]/5mL & nbsp;   HEPARIN SODIUM
Administration Route(s): INTRAVENOUS
Dosage Form(s): INJECTION, SOLUTION, CONCENTRATE
Coding System: National Drug Codes(NDC)

Labeler Information of Heparin Sodium

Product NDC: 0409-2581
Labeler Name: Hospira, Inc.
Product Type: HUMAN PRESCRIPTION DRUG
FDA Application Number: NDA005264
Marketing Category: NDA
Start Marketing Date: 20101022

Package Information of Heparin Sodium

Package NDC: 0409-2581-02
Package Description: 25 VIAL, PATENT DELIVERY SYSTEM in 1 TRAY (0409-2581-02) > 5 mL in 1 VIAL, PATENT DELIVERY SYSTEM

NDC Information of Heparin Sodium

NDC Code 0409-2581-02
Proprietary Name Heparin Sodium
Package Description 25 VIAL, PATENT DELIVERY SYSTEM in 1 TRAY (0409-2581-02) > 5 mL in 1 VIAL, PATENT DELIVERY SYSTEM
Product NDC 0409-2581
Product Type Name HUMAN PRESCRIPTION DRUG
Non Proprietary Name HEPARIN SODIUM
Dosage Form Name INJECTION, SOLUTION, CONCENTRATE
Route Name INTRAVENOUS
Start Marketing Date 20101022
Marketing Category Name NDA
Labeler Name Hospira, Inc.
Substance Name HEPARIN SODIUM
Strength Number 10000
Strength Unit [USP'U]/5mL
Pharmaceutical Classes Anti-coagulant [EPC],Heparin [Chemical/Ingredient],Unfractionated Heparin [EPC]

Complete Information of Heparin Sodium


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