This brand name is authorized in Australia, Austria, Brazil, Croatia, Cyprus, Estonia, France, Hong Kong SAR China, Ireland, Israel, Italy, Lithuania, Netherlands, New Zealand, Poland, Romania, Singapore, Spain, Turkey.
The drug ELONVA contains one active pharmaceutical ingredient (API):
1
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UNII
T7K20Y2GWY - CORIFOLLITROPIN ALFA
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Corifollitropin alfa is designed as a sustained follicle stimulant with the same pharmacodynamic profile as (rec)FSH, but with a markedly prolonged duration of FSH activity. Corifollitropin alfa does not display any intrinsic LH/hCG activity. |
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Below package inserts are available for further reading:
| Document | Type | Information Source | |
|---|---|---|---|
| ELONVA Solution for injection | MPI, EU: SmPC | European Medicines Agency (EU) |
This drug has been classified in the anatomical therapeutic chemical (ATC) classification system as follows:
| ATC Group | Classification | |
|---|---|---|
| G03GA09 | Corifollitropin alfa | 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) |
|---|---|---|
| AU | Pharmaceutical Benefits Scheme | 5816D, 5817E |
| BR | Câmara de Regulação do Mercado de Medicamentos | 527304701150316, 527304702157314 |
| EE | Ravimiamet | 1459357, 1459391 |
| ES | Centro de información online de medicamentos de la AEMPS | 09609001, 09609002 |
| FR | Base de données publique des médicaments | 64036190, 66844562 |
| HK | Department of Health Drug Office | 60584, 60585 |
| IL | מִשְׂרַד הַבְּרִיאוּת | 6675, 6676 |
| IT | Agenzia del Farmaco | 039943016, 039943028 |
| LT | Valstybinė vaistų kontrolės tarnyba | 1053070, 1053071 |
| NL | Z-Index G-Standaard, PRK | 138126, 138134 |
| NZ | Medicines and Medical Devices Safety Authority | 13913, 14010 |
| PL | Rejestru Produktów Leczniczych | 100230783, 100230790 |
| RO | Agenția Națională a Medicamentului și a Dispozitivelor Medicale | W67764001 |
| SG | Health Sciences Authority | 13939P, 13940P |
| TR | İlaç ve Tıbbi Cihaz Kurumu | 8683280337145, 8683280337152 |
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