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FONDAPARINUX SODIUM - 60505-6080-4 - (fondaparinux sodium)

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Drug Information of FONDAPARINUX SODIUM

Product NDC: 60505-6080
Proprietary Name: FONDAPARINUX SODIUM
Non Proprietary Name: fondaparinux sodium
Active Ingredient(s): 7.5    mg/.6mL & nbsp;   fondaparinux sodium
Administration Route(s): SUBCUTANEOUS
Dosage Form(s): INJECTION, SOLUTION
Coding System: National Drug Codes(NDC)

Labeler Information of FONDAPARINUX SODIUM

Product NDC: 60505-6080
Labeler Name: Apotex Corp.
Product Type: HUMAN PRESCRIPTION DRUG
FDA Application Number: NDA021345
Marketing Category: NDA
Start Marketing Date: 20110718

Package Information of FONDAPARINUX SODIUM

Package NDC: 60505-6080-4
Package Description: 10 SYRINGE in 1 CARTON (60505-6080-4) > .6 mL in 1 SYRINGE (60505-6080-0)

NDC Information of FONDAPARINUX SODIUM

NDC Code 60505-6080-4
Proprietary Name FONDAPARINUX SODIUM
Package Description 10 SYRINGE in 1 CARTON (60505-6080-4) > .6 mL in 1 SYRINGE (60505-6080-0)
Product NDC 60505-6080
Product Type Name HUMAN PRESCRIPTION DRUG
Non Proprietary Name fondaparinux sodium
Dosage Form Name INJECTION, SOLUTION
Route Name SUBCUTANEOUS
Start Marketing Date 20110718
Marketing Category Name NDA
Labeler Name Apotex Corp.
Substance Name FONDAPARINUX SODIUM
Strength Number 7.5
Strength Unit mg/.6mL
Pharmaceutical Classes Factor Xa Inhibitor [EPC],Factor Xa Inhibitors [MoA]

Complete Information of FONDAPARINUX SODIUM


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