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Fondaparinux Sodium - 55111-678-10 - (Fondaparinux Sodium)

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Drug Information of Fondaparinux Sodium

Product NDC: 55111-678
Proprietary Name: Fondaparinux Sodium
Non Proprietary Name: Fondaparinux Sodium
Active Ingredient(s): 2.5    mg/.5mL & nbsp;   Fondaparinux Sodium
Administration Route(s): SUBCUTANEOUS
Dosage Form(s): INJECTION
Coding System: National Drug Codes(NDC)

Labeler Information of Fondaparinux Sodium

Product NDC: 55111-678
Labeler Name: Dr. Reddy's Laboratories Limited
Product Type: HUMAN PRESCRIPTION DRUG
FDA Application Number: ANDA091316
Marketing Category: ANDA
Start Marketing Date: 20110714

Package Information of Fondaparinux Sodium

Package NDC: 55111-678-10
Package Description: 10 SYRINGE in 1 CARTON (55111-678-10) > .5 mL in 1 SYRINGE (55111-678-11)

NDC Information of Fondaparinux Sodium

NDC Code 55111-678-10
Proprietary Name Fondaparinux Sodium
Package Description 10 SYRINGE in 1 CARTON (55111-678-10) > .5 mL in 1 SYRINGE (55111-678-11)
Product NDC 55111-678
Product Type Name HUMAN PRESCRIPTION DRUG
Non Proprietary Name Fondaparinux Sodium
Dosage Form Name INJECTION
Route Name SUBCUTANEOUS
Start Marketing Date 20110714
Marketing Category Name ANDA
Labeler Name Dr. Reddy's Laboratories Limited
Substance Name FONDAPARINUX SODIUM
Strength Number 2.5
Strength Unit mg/.5mL
Pharmaceutical Classes Factor Xa Inhibitor [EPC],Factor Xa Inhibitors [MoA]

Complete Information of Fondaparinux Sodium


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