This brand name is authorized in Austria, Brazil, Canada, Croatia, Ecuador, Estonia, Finland, France, Ireland, Israel, Italy, Lithuania, Mexico, Netherlands, Poland, Romania, Singapore, South Africa, Spain, UK.
The drug EVRA contains a combination of these active pharmaceutical ingredients (APIs):
1
|
UNII
R0TAY3X631 - NORELGESTROMIN
|
2
|
UNII
423D2T571U - ETHINYL ESTRADIOL
|
|
Ethinylestradiol is chemically and biologically identical to endogenous human oestradiol. It substitutes for the loss of estrogen production in menopausal women, and alleviates menopausal symptoms. Estrogens prevent bone loss following menopause or ovariectomy. |
|
Below package inserts are available for further reading:
| Document | Type | Information Source | |
|---|---|---|---|
| EVRA Plaster | 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 | |
|---|---|---|
| G03AA13 | Norelgestromin and ethinylestradiol | G Genito urinary system and sex hormones → G03 Sex hormones and modulators of the genital system → G03A Hormonal contraceptives for systemic use → G03AA Progestogens and estrogens, fixed combinations |
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 | 514500701174311 |
| CA | Health Products and Food Branch | 02248297 |
| EC | Agencia Nacional de Regulación, Control y Vigilancia Sanitaria | 26.190-02-05 |
| EE | Ravimiamet | 1131589, 1131590, 1131602 |
| ES | Centro de información online de medicamentos de la AEMPS | 02223001, 02223001IP, 02223001IP1, 02223001IP2, 02223001IP3, 02223001IP4, 02223002, 02223002IP1, 02223002IP2, 02223002IP3 |
| FI | Lääkealan turvallisuus- ja kehittämiskeskus | 012921, 013101, 013107 |
| FR | Base de données publique des médicaments | 69729088 |
| GB | Medicines & Healthcare Products Regulatory Agency | 46088 |
| IE | Health Products Regulatory Authority | 24402, 24408 |
| IL | מִשְׂרַד הַבְּרִיאוּת | 4723, 4724 |
| IT | Agenzia del Farmaco | 035684012, 035684024, 035684036, 045753011, 048236018, 049088014 |
| LT | Valstybinė vaistų kontrolės tarnyba | 1012652, 1012653, 1012654 |
| MX | Comisión Federal para la Protección contra Riesgos Sanitarios | 381M2002 |
| NL | Z-Index G-Standaard | 14810735 |
| NL | Z-Index G-Standaard, PRK | 121711 |
| PL | Rejestru Produktów Leczniczych | 100113907 |
| RO | Agenția Națională a Medicamentului și a Dispozitivelor Medicale | W68023001, W68023002, W68023003 |
| SG | Health Sciences Authority | 12423P |
| ZA | Health Products Regulatory Authority | 36/18.7/0491 |
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