This brand name is authorized in Estonia, Ireland, Lithuania, Poland, Romania, United Kingdom
The drug ZIBOR contains one active pharmaceutical ingredient (API):
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1
Bemiparin
UNII P59JKU02CE - BEMIPARIN SODIUM
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Bemiparin is a LMWH obtained by depolymerization of heparin from porcine intestinal mucosa. Bemiparin has confirmed its antithrombotic activity and, at the recommended doses, it does not significantly prolong global clotting tests. |
Below package inserts are available for further reading:
| Title | Information Source | Document Type | |
|---|---|---|---|
| ZIBOR 3.500 IU Solution for injection | Health Products Regulatory Authority (IE) | MPI, EU: SmPC | |
| ZIBOR 25.000 IU Solution for injection | Health Products Regulatory Authority (IE) | MPI, EU: SmPC | |
| ZIBOR 2.500 IU Solution for injection | Health Products Regulatory Authority (IE) | MPI, EU: SmPC |
This drug has been classified in the anatomical therapeutic chemical (ATC) classification system as follows:
| ATC code | Group title | Classification |
|---|---|---|
| B01AB12 | Bemiparin | B Blood and blood forming organs → B01 Antithrombotic agents → B01A Antithrombotic agents → B01AB Heparin group |
This drug has been assigned below unique identifiers within the countries it is being marketed:
| Country | Identification scheme | Identifier(s) |
|---|---|---|
| Country: EE | Ravimiamet | Identifier(s): 1193105, 1193116, 1193127, 1193138, 1193149, 1193150, 1193161, 1193172, 1193183, 1193194, 1247947, 1247958, 1247969, 1247970, 1454879, 1455207, 1455218, 1455229, 1455230, 1455241, 1455252, 1455263 |
| Country: GB | Medicines & Healthcare Products Regulatory Agency | Identifier(s): 395671, 395673 |
| Country: LT | Valstybinė vaistų kontrolės tarnyba | Identifier(s): 1021141, 1021142, 1021143, 1021144, 1021145, 1021147, 1021148, 1021149, 1021150, 1021151, 1023300, 1025730, 1025731, 1025732, 1025733, 1025734, 1025735, 1025736, 1025737, 1025738, 1025739, 1025740, 1085603, 1085604 |
| Country: PL | Rejestru Produktów Leczniczych | Identifier(s): 100006198, 100160806, 100160835 |
| Country: RO | Agenția Națională a Medicamentului și a Dispozitivelor Medicale | Identifier(s): W68540001, W68540002, W68540003, W68540004, W68541001, W68541002, W68541003, W68541004, W68542001, W68542002, W68542003, W68542004, W68542005, W68542006, W68542007, W68542008, W68542009, W68542010, W68542011, W68542012 |
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