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Enoxaparin Sodium - 0781-3119-68 - (Enoxaparin Sodium)

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Drug Information of Enoxaparin Sodium

Product NDC: 0781-3119
Proprietary Name: Enoxaparin Sodium
Non Proprietary Name: Enoxaparin Sodium
Active Ingredient(s): 100    mg/mL & nbsp;   Enoxaparin Sodium
Administration Route(s): SUBCUTANEOUS
Dosage Form(s): INJECTION
Coding System: National Drug Codes(NDC)

Labeler Information of Enoxaparin Sodium

Product NDC: 0781-3119
Labeler Name: Sandoz Inc
Product Type: HUMAN PRESCRIPTION DRUG
FDA Application Number: ANDA077857
Marketing Category: ANDA
Start Marketing Date: 20100723

Package Information of Enoxaparin Sodium

Package NDC: 0781-3119-68
Package Description: 10 SYRINGE in 1 CARTON (0781-3119-68) > .8 mL in 1 SYRINGE (0781-3119-04)

NDC Information of Enoxaparin Sodium

NDC Code 0781-3119-68
Proprietary Name Enoxaparin Sodium
Package Description 10 SYRINGE in 1 CARTON (0781-3119-68) > .8 mL in 1 SYRINGE (0781-3119-04)
Product NDC 0781-3119
Product Type Name HUMAN PRESCRIPTION DRUG
Non Proprietary Name Enoxaparin Sodium
Dosage Form Name INJECTION
Route Name SUBCUTANEOUS
Start Marketing Date 20100723
Marketing Category Name ANDA
Labeler Name Sandoz Inc
Substance Name ENOXAPARIN SODIUM
Strength Number 100
Strength Unit mg/mL
Pharmaceutical Classes Heparin, Low-Molecular-Weight [Chemical/Ingredient],Low Molecular Weight Heparin [EPC]

Complete Information of Enoxaparin Sodium


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