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Heparin Sodium - 52584-262-01 - (Heparin Sodium)

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Drug Information of Heparin Sodium

Product NDC: 52584-262
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: 52584-262
Labeler Name: General Injectables & Vaccines, Inc
Product Type: HUMAN PRESCRIPTION DRUG
FDA Application Number: NDA017029
Marketing Category: NDA
Start Marketing Date: 20100801

Package Information of Heparin Sodium

Package NDC: 52584-262-01
Package Description: 1 VIAL, MULTI-DOSE in 1 BAG (52584-262-01) > 1 mL in 1 VIAL, MULTI-DOSE

NDC Information of Heparin Sodium

NDC Code 52584-262-01
Proprietary Name Heparin Sodium
Package Description 1 VIAL, MULTI-DOSE in 1 BAG (52584-262-01) > 1 mL in 1 VIAL, MULTI-DOSE
Product NDC 52584-262
Product Type Name HUMAN PRESCRIPTION DRUG
Non Proprietary Name Heparin Sodium
Dosage Form Name INJECTION, SOLUTION
Route Name INTRAVENOUS; SUBCUTANEOUS
Start Marketing Date 20100801
Marketing Category Name NDA
Labeler Name General Injectables & Vaccines, Inc
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


General Information