Lovenox - 0075-0623-01 - (enoxaparin sodium)

Alphabetical Index


Drug Information of Lovenox

Product NDC: 0075-0623
Proprietary Name: Lovenox
Non Proprietary Name: enoxaparin sodium
Active Ingredient(s): 100    mg/mL & nbsp;   enoxaparin sodium
Administration Route(s): INTRAVENOUS; SUBCUTANEOUS
Dosage Form(s): INJECTION
Coding System: National Drug Codes(NDC)

Labeler Information of Lovenox

Product NDC: 0075-0623
Labeler Name: sanofi-aventis U.S. LLC
Product Type: HUMAN PRESCRIPTION DRUG
FDA Application Number: NDA020164
Marketing Category: NDA
Start Marketing Date: 19930329

Package Information of Lovenox

Package NDC: 0075-0623-01
Package Description: 10 SYRINGE in 1 CARTON (0075-0623-01) > 1 mL in 1 SYRINGE

NDC Information of Lovenox

NDC Code 0075-0623-01
Proprietary Name Lovenox
Package Description 10 SYRINGE in 1 CARTON (0075-0623-01) > 1 mL in 1 SYRINGE
Product NDC 0075-0623
Product Type Name HUMAN PRESCRIPTION DRUG
Non Proprietary Name enoxaparin sodium
Dosage Form Name INJECTION
Route Name INTRAVENOUS; SUBCUTANEOUS
Start Marketing Date 19930329
Marketing Category Name NDA
Labeler Name sanofi-aventis U.S. LLC
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 Lovenox


General Information