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Heparin Sodium - 63323-262-01 - (HEPARIN SODIUM)

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Drug Information of Heparin Sodium

Product NDC: 63323-262
Proprietary Name: Heparin Sodium
Non Proprietary Name: HEPARIN SODIUM
Active Ingredient(s): 5000    [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: 63323-262
Labeler Name: APP Pharmaceuticals, LLC
Product Type: HUMAN PRESCRIPTION DRUG
FDA Application Number: NDA017029
Marketing Category: NDA
Start Marketing Date: 20090812

Package Information of Heparin Sodium

Package NDC: 63323-262-01
Package Description: 25 VIAL in 1 TRAY (63323-262-01) > 1 mL in 1 VIAL

NDC Information of Heparin Sodium

NDC Code 63323-262-01
Proprietary Name Heparin Sodium
Package Description 25 VIAL in 1 TRAY (63323-262-01) > 1 mL in 1 VIAL
Product NDC 63323-262
Product Type Name HUMAN PRESCRIPTION DRUG
Non Proprietary Name HEPARIN SODIUM
Dosage Form Name INJECTION, SOLUTION
Route Name INTRAVENOUS; SUBCUTANEOUS
Start Marketing Date 20090812
Marketing Category Name NDA
Labeler Name APP Pharmaceuticals, LLC
Substance Name HEPARIN SODIUM
Strength Number 5000
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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