Enoxaparin Other names: Enoxaparin sodium
Active ingredient description
Enoxaparin is a LMWH with a mean molecular weight of approximately 4,500 daltons, in which the antithrombotic and anticoagulant activities of standard heparin have been dissociated. The drug substance is the sodium salt and has a high anti-Xa activity.
Medicine classification
This medicinal substance has been classified in the anatomical therapeutic chemical (ATC) classification according to its main therapeutic use as follows:
| ATC Group | Classification | |
|---|---|---|
| B01AB05 | Enoxaparin | B Blood and blood forming organs → B01 Antithrombotic agents → B01A Antithrombotic agents → B01AB Heparin group |
Product monographs
Competent medicine agencies globally have authorized commercialization of this active ingredient according to these medication package inserts (MPIs):
| Document | Type | Information Source | |
|---|---|---|---|
| LOVENOX Solution for injection | MPI, US: SPL/PLR | FDA, National Drug Code (US) | |
| AROVI 2,000 IU Solution for injection in pre-filled syringe | MPI, EU: SmPC | Medicines & Healthcare Products Regulatory Agency (GB) |
Medicines
Enoxaparin is an active ingredient of these brands:
Albania (AL)
Australia (AU)
Austria (AT)
Brazil (BR)
Canada (CA)
Croatia (HR)Cyprus (CY)Ecuador (EC)
Estonia (EE)
Finland (FI)France (FR)Germany (DE)
Hong Kong (HK)
Ireland (IE)
Israel (IL)Italy (IT)
Japan (JP)
Lithuania (LT)Malta (MT)
Mexico (MX)
Netherlands (NL)New Zealand (NZ)Nigeria (NG)Poland (PL)
Romania (RO)
Singapore (SG)
South Africa (ZA)
Spain (ES)Tunisia (TN)Turkey (TR)
United Kingdom (UK)United States (US)
Note the following: The list of brand names is continuously updated, and thus does not include the total of products circulating worldwide. |
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