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Enoxaparin sodium - 0955-1016-01 - (enoxaparin sodium)

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Drug Information of Enoxaparin sodium

Product NDC: 0955-1016
Proprietary Name: Enoxaparin sodium
Non Proprietary Name: enoxaparin sodium
Active Ingredient(s): 300    mg/3mL & nbsp;   enoxaparin sodium
Administration Route(s): SUBCUTANEOUS
Dosage Form(s): INJECTION
Coding System: National Drug Codes(NDC)

Labeler Information of Enoxaparin sodium

Product NDC: 0955-1016
Labeler Name: Winthrop U.S.
Product Type: HUMAN PRESCRIPTION DRUG
FDA Application Number: NDA020164
Marketing Category: NDA AUTHORIZED GENERIC
Start Marketing Date: 20111003

Package Information of Enoxaparin sodium

Package NDC: 0955-1016-01
Package Description: 1 VIAL, MULTI-DOSE in 1 CARTON (0955-1016-01) > 3 mL in 1 VIAL, MULTI-DOSE

NDC Information of Enoxaparin sodium

NDC Code 0955-1016-01
Proprietary Name Enoxaparin sodium
Package Description 1 VIAL, MULTI-DOSE in 1 CARTON (0955-1016-01) > 3 mL in 1 VIAL, MULTI-DOSE
Product NDC 0955-1016
Product Type Name HUMAN PRESCRIPTION DRUG
Non Proprietary Name enoxaparin sodium
Dosage Form Name INJECTION
Route Name SUBCUTANEOUS
Start Marketing Date 20111003
Marketing Category Name NDA AUTHORIZED GENERIC
Labeler Name Winthrop U.S.
Substance Name ENOXAPARIN SODIUM
Strength Number 300
Strength Unit mg/3mL
Pharmaceutical Classes Heparin, Low-Molecular-Weight [Chemical/Ingredient],Low Molecular Weight Heparin [EPC]

Complete Information of Enoxaparin sodium


General Information