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Heparin Sodium - 55154-9360-5 - (HEPARIN SODIUM)

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Drug Information of Heparin Sodium

Product NDC: 55154-9360
Proprietary Name: Heparin Sodium
Non Proprietary Name: HEPARIN SODIUM
Active Ingredient(s): 1000    [USP'U]/mL & nbsp;   HEPARIN SODIUM
Administration Route(s): INTRAVENOUS; SUBCUTANEOUS
Dosage Form(s): INJECTION, SOLUTION
Coding System: National Drug Codes(NDC)

Labeler Information of Heparin Sodium

Product NDC: 55154-9360
Labeler Name: Cardinal Health
Product Type: HUMAN PRESCRIPTION DRUG
FDA Application Number: NDA017029
Marketing Category: NDA
Start Marketing Date: 20100618

Package Information of Heparin Sodium

Package NDC: 55154-9360-5
Package Description: 5 VIAL in 1 BAG (55154-9360-5) > 10 mL in 1 VIAL

NDC Information of Heparin Sodium

NDC Code 55154-9360-5
Proprietary Name Heparin Sodium
Package Description 5 VIAL in 1 BAG (55154-9360-5) > 10 mL in 1 VIAL
Product NDC 55154-9360
Product Type Name HUMAN PRESCRIPTION DRUG
Non Proprietary Name HEPARIN SODIUM
Dosage Form Name INJECTION, SOLUTION
Route Name INTRAVENOUS; SUBCUTANEOUS
Start Marketing Date 20100618
Marketing Category Name NDA
Labeler Name Cardinal Health
Substance Name HEPARIN SODIUM
Strength Number 1000
Strength Unit [USP'U]/mL
Pharmaceutical Classes Anti-coagulant [EPC],Heparin [Chemical/Ingredient],Unfractionated Heparin [EPC]

Complete Information of Heparin Sodium


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