This brand name is authorized in Austria, Brazil, Canada, Croatia, Cyprus, Estonia, Finland, France, Hong Kong SAR China, Ireland, Israel, Japan, Lithuania, Netherlands, New Zealand, Poland, Romania, Singapore, Spain, Tunisia, Turkey, UK.
The drug ADVATE 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) |
|---|---|---|
| BR | Câmara de Regulação do Mercado de Medicamentos | 501121010033917, 501121010034017, 501121010034117, 501121010034217 |
| CA | Health Products and Food Branch | 02284154, 02284162, 02313111, 02337193, 02365944, 02365952 |
| EE | Ravimiamet | 1204164, 1204175, 1204186, 1204197, 1362507, 1362518, 1552834, 1552845, 1552856, 1552867 |
| ES | Centro de información online de medicamentos de la AEMPS | 03271003, 103271015, 103271016, 103271017, 103271018, 103271019, 103271020 |
| FI | Lääkealan turvallisuus- ja kehittämiskeskus | 048784, 057458, 076358, 442678, 458666, 564270 |
| FR | Base de données publique des médicaments | 64445956, 66954464, 67778827, 68255655, 68294455, 69558317 |
| GB | Medicines & Healthcare Products Regulatory Agency | 139117, 139120, 391594, 391601, 391603, 391605, 76583, 76587 |
| HK | Department of Health Drug Office | 56259, 56260, 56371, 56372 |
| IL | מִשְׂרַד הַבְּרִיאוּת | 8093 |
| JP | 医薬品医療機器総合機構 | 6343432G1025, 6343432G2021, 6343432G3028, 6343432G4024, 6343432G5020, 6343432G6027 |
| LT | Valstybinė vaistų kontrolės tarnyba | 1005041, 1005042, 1005043, 1005044, 1032840, 1032841, 1064524, 1064525, 1064526, 1064527, 1074982, 1074983, 1074984, 1074985, 1074986, 1074987, 1074988, 1074989, 1074990, 1074991 |
| NL | Z-Index G-Standaard | 14934590, 14934612, 14934620 |
| NL | Z-Index G-Standaard, PRK | 67032, 67040, 67059, 72788, 86649, 86657 |
| NZ | Medicines and Medical Devices Safety Authority | 11644, 11645, 11646, 11647, 13224, 13246, 16293 |
| PL | Rejestru Produktów Leczniczych | 100139309, 100139321, 100139338, 100139344, 100208625, 100208631 |
| RO | Agenția Națională a Medicamentului și a Dispozitivelor Medicale | W66730001, W66731001, W66732001, W66733001, W66734001, W66735001, W66735002, W69203001, W69204001, W69205001, W69206001 |
| SG | Health Sciences Authority | 13492P, 13493P, 13496P, 13497P |
| TN | Direction de la Pharmacie et du Médicament | 10623081H, 10623082H, 10623083H |
| TR | İlaç ve Tıbbi Cihaz Kurumu | 8681429550004, 8681429550011, 8681429550028, 8681429550035, 8681429550042, 8681429550059 |
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