This brand name is authorized in Austria, Cyprus, Estonia, Ireland, Lithuania, Netherlands, New Zealand, Poland, Singapore, South Africa, Tunisia.
The drug KOGENATE contains one active pharmaceutical ingredient (API):
1
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UNII
P89DR4NY54 - ANTIHEMOPHILIC FACTOR, HUMAN RECOMBINANT
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Octocog alfa (Full length recombinant human coagulation factor VIII (rDNA)) is a purified protein that has 2,332 amino acids. It is produced by recombinant DNA technology in baby hamster kidney cells (BHK) into which the human factor VIII gene has been introduced. |
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This drug has been classified in the anatomical therapeutic chemical (ATC) classification system as follows:
| ATC Group | Classification | |
|---|---|---|
| B02BD02 | Coagulation factor VIII | B Blood and blood forming organs → B02 Antihemorrhagics → B02B Vitamin K and other hemostatics → B02BD Blood coagulation factors |
This drug has been assigned below unique identifiers within the countries it is being marketed:
| Country | Identification scheme | Identifier(s) |
|---|---|---|
| EE | Ravimiamet | 1202634, 1202656, 1202678, 1367366, 1489125 |
| LT | Valstybinė vaistų kontrolės tarnyba | 1004818, 1004819, 1004820, 1005121, 1029335, 1029340, 1029342, 1031803, 1056129, 1056130 |
| NL | Z-Index G-Standaard, PRK | 57673, 57681, 57703, 85731 |
| NZ | Medicines and Medical Devices Safety Authority | 13345, 14580, 8511, 8512, 8513 |
| PL | Rejestru Produktów Leczniczych | 100127170, 100127186, 100127192, 100188992, 100235384 |
| SG | Health Sciences Authority | 13385P, 13386P, 13387P |
| TN | Direction de la Pharmacie et du Médicament | 12693011H, 12693012H, 12693013H |
| ZA | Health Products Regulatory Authority | 29/8.1/0009, 29/8.1/0010, 29/8.1/0011, 41/8.1/1086, 41/8.1/1087, 41/8.1/1088 |
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