This brand name is authorized in Austria, Brazil, Cyprus, Ecuador, Finland, France, Ireland, Israel, Malta, Netherlands, Poland, South Africa, Tunisia, Turkey, UK.
The drug FOSTIMON contains one active pharmaceutical ingredient (API):
1
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UNII
W9BB98U6HP - UROFOLLITROPIN
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Urofollitropin contains a highly purified preparation of urinary FSH extracted from the urine of postmenopausal women. FSH stimulates ovarian follicular growth and development as well as gonadal steroid production in women who do not have primary ovarian failure. |
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Below package inserts are available for further reading:
| Document | Type | Information Source | |
|---|---|---|---|
| FOSTIMON Powder and solvent for solution for injection | 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 | |
|---|---|---|
| G03GA04 | Urofollitropin | G Genito urinary system and sex hormones → G03 Sex hormones and modulators of the genital system → G03G Gonadotropins and other ovulation stimulants → G03GA Gonadotropins |
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 | 525213050018604, 525213050018704, 525213050018804, 525213050018904, 525213050019004, 525213050019104 |
| EC | Agencia Nacional de Regulación, Control y Vigilancia Sanitaria | 22.453-1-01-06, 22.455-1-01-06 |
| FI | Lääkealan turvallisuus- ja kehittämiskeskus | 054768, 415813, 531676, 580901 |
| FR | Base de données publique des médicaments | 60549797, 61166549, 62712912, 69325035 |
| GB | Medicines & Healthcare Products Regulatory Agency | 108913, 108921 |
| IL | מִשְׂרַד הַבְּרִיאוּת | 6065, 6066 |
| MT | Medicines Authority | AA770/08601 |
| NL | Z-Index G-Standaard | 15858693 |
| NL | Z-Index G-Standaard, PRK | 104531, 116319, 121517, 82414 |
| PL | Rejestru Produktów Leczniczych | 100087044 |
| TN | Direction de la Pharmacie et du Médicament | 13533011, 13533012 |
| TR | İlaç ve Tıbbi Cihaz Kurumu | 8680426040013, 8680426040020, 8680426040075, 8680426040082 |
| ZA | Health Products Regulatory Authority | 42/21.10/0184 |
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