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Heparin Sodium - 52584-581-02 - (Heparin Sodium)

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Drug Information of Heparin Sodium

Product NDC: 52584-581
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: 52584-581
Labeler Name: General Injectables & Vaccines, Inc
Product Type: HUMAN PRESCRIPTION DRUG
FDA Application Number: NDA005264
Marketing Category: NDA
Start Marketing Date: 20100301

Package Information of Heparin Sodium

Package NDC: 52584-581-02
Package Description: 1 VIAL in 1 BAG (52584-581-02) > 5 mL in 1 VIAL

NDC Information of Heparin Sodium

NDC Code 52584-581-02
Proprietary Name Heparin Sodium
Package Description 1 VIAL in 1 BAG (52584-581-02) > 5 mL in 1 VIAL
Product NDC 52584-581
Product Type Name HUMAN PRESCRIPTION DRUG
Non Proprietary Name Heparin Sodium
Dosage Form Name INJECTION, SOLUTION, CONCENTRATE
Route Name INTRAVENOUS
Start Marketing Date 20100301
Marketing Category Name NDA
Labeler Name General Injectables & Vaccines, 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


General Information