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Enoxaparin Sodium - 62037-861-20 - (Enoxaparin Sodium)

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Drug Information of Enoxaparin Sodium

Product NDC: 62037-861
Proprietary Name: Enoxaparin Sodium
Non Proprietary Name: Enoxaparin Sodium
Active Ingredient(s): 60    mg/.6mL & nbsp;   Enoxaparin Sodium
Administration Route(s): SUBCUTANEOUS
Dosage Form(s): INJECTION
Coding System: National Drug Codes(NDC)

Labeler Information of Enoxaparin Sodium

Product NDC: 62037-861
Labeler Name: Watson Pharma, Inc.
Product Type: HUMAN PRESCRIPTION DRUG
FDA Application Number: ANDA076684
Marketing Category: ANDA
Start Marketing Date: 20120127

Package Information of Enoxaparin Sodium

Package NDC: 62037-861-20
Package Description: 10 BLISTER PACK in 1 CARTON (62037-861-20) > 1 SYRINGE in 1 BLISTER PACK > .6 mL in 1 SYRINGE

NDC Information of Enoxaparin Sodium

NDC Code 62037-861-20
Proprietary Name Enoxaparin Sodium
Package Description 10 BLISTER PACK in 1 CARTON (62037-861-20) > 1 SYRINGE in 1 BLISTER PACK > .6 mL in 1 SYRINGE
Product NDC 62037-861
Product Type Name HUMAN PRESCRIPTION DRUG
Non Proprietary Name Enoxaparin Sodium
Dosage Form Name INJECTION
Route Name SUBCUTANEOUS
Start Marketing Date 20120127
Marketing Category Name ANDA
Labeler Name Watson Pharma, Inc.
Substance Name ENOXAPARIN SODIUM
Strength Number 60
Strength Unit mg/.6mL
Pharmaceutical Classes Heparin, Low-Molecular-Weight [Chemical/Ingredient],Low Molecular Weight Heparin [EPC]

Complete Information of Enoxaparin Sodium


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