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Heparin Sodium - 0409-1316-25 - (HEPARIN SODIUM)

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Drug Information of Heparin Sodium

Product NDC: 0409-1316
Proprietary Name: Heparin Sodium
Non Proprietary Name: HEPARIN SODIUM
Active Ingredient(s): 10000    [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: 0409-1316
Labeler Name: Hospira, Inc.
Product Type: HUMAN PRESCRIPTION DRUG
FDA Application Number: ANDA089522
Marketing Category: ANDA
Start Marketing Date: 19870504

Package Information of Heparin Sodium

Package NDC: 0409-1316-25
Package Description: 10 SYRINGE in 1 CARTON (0409-1316-25) > .5 mL in 1 SYRINGE

NDC Information of Heparin Sodium

NDC Code 0409-1316-25
Proprietary Name Heparin Sodium
Package Description 10 SYRINGE in 1 CARTON (0409-1316-25) > .5 mL in 1 SYRINGE
Product NDC 0409-1316
Product Type Name HUMAN PRESCRIPTION DRUG
Non Proprietary Name HEPARIN SODIUM
Dosage Form Name INJECTION, SOLUTION
Route Name INTRAVENOUS; SUBCUTANEOUS
Start Marketing Date 19870504
Marketing Category Name ANDA
Labeler Name Hospira, Inc.
Substance Name HEPARIN SODIUM
Strength Number 10000
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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