This brand name is authorized in United States. It is also authorized in Australia, France, Hong Kong SAR China, Ireland, Netherlands, New Zealand, Poland, Singapore, Spain, Turkey, UK.
The drug VELETRI contains one active pharmaceutical ingredient (API):
1
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UNII
DCR9Z582X0 - EPOPROSTENOL
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Epoprostenol sodium, the monosodium salt of epoprostenol, a naturally occurring prostaglandin produced by the intima of blood vessels. Epoprostenol is the most potent inhibitor of platelet aggregation known. It is also a potent vasodilator. |
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Below package inserts are available for further reading:
| Document | Type | Information Source | |
|---|---|---|---|
| VELETRI Powder for solution for infusion | MPI, EU: SmPC | Medicines & Healthcare Products Regulatory Agency (GB) |
This drug has been classified in the anatomical therapeutic chemical (ATC) classification system as follows:
| ATC Group | Classification | |
|---|---|---|
| B01AC09 | Epoprostenol | B Blood and blood forming organs → B01 Antithrombotic agents → B01A Antithrombotic agents → B01AC Platelet aggregation inhibitors excl. heparin |
This drug has been assigned below unique identifiers within the countries it is being marketed:
| Country | Identification scheme | Identifier(s) |
|---|---|---|
| AU | Pharmaceutical Benefits Scheme | 10111E, 10117L, 10129D, 10130E |
| ES | Centro de información online de medicamentos de la AEMPS | 81076, 81077 |
| FR | Base de données publique des médicaments | 60181231, 69903585 |
| GB | Medicines & Healthcare Products Regulatory Agency | 226474, 226477 |
| HK | Department of Health Drug Office | 66503, 66504 |
| IE | Health Products Regulatory Authority | 88772, 88773 |
| NL | Z-Index G-Standaard, PRK | 33898, 52809 |
| NZ | Medicines and Medical Devices Safety Authority | 16506, 16507 |
| PL | Rejestru Produktów Leczniczych | 100304694, 100304702 |
| SG | Health Sciences Authority | 15405P, 15406P |
| TR | İlaç ve Tıbbi Cihaz Kurumu | 8699593270017, 8699593270024 |
| US | FDA, National Drug Code | 66215-402, 66215-403 |
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