This brand name is authorized in Austria, Croatia, Cyprus, Estonia, Finland, France, Ireland, Israel, Italy, Japan, Lithuania, Netherlands, Poland, Romania, Spain, Turkey, UK.
The drug SELINCRO contains one active pharmaceutical ingredient (API):
1
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UNII
K7K69QC05X - NALMEFENE HYDROCHLORIDE
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Nalmefene is an opioid system modulator with a distinct μ, δ, and κ receptor profile. Nalmefene is indicated for the reduction of alcohol consumption in adult patients with alcohol dependence, without physical withdrawal symptoms and who do not require immediate detoxification. |
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Below package inserts are available for further reading:
| Document | Type | Information Source | |
|---|---|---|---|
| SELINCRO Film-coated tablet | 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 | |
|---|---|---|
| N07BB05 | N Nervous system → N07 Other nervous system drugs → N07B Drugs used in addictive disorders → N07BB Drugs used in alcohol dependence | |
This drug has been assigned below unique identifiers within the countries it is being marketed:
| Country | Identification scheme | Identifier(s) |
|---|---|---|
| EE | Ravimiamet | 1608982, 1608993, 1609006, 1609017, 1609028, 1650495 |
| ES | Centro de información online de medicamentos de la AEMPS | 112815002 |
| FI | Lääkealan turvallisuus- ja kehittämiskeskus | 138603, 187057, 491998, 580104 |
| FR | Base de données publique des médicaments | 63957761 |
| GB | Medicines & Healthcare Products Regulatory Agency | 223684, 223685 |
| IE | Health Products Regulatory Authority | 54344, 54345 |
| IL | מִשְׂרַד הַבְּרִיאוּת | 7412, 7413, 7414 |
| IT | Agenzia del Farmaco | 042683019, 042683021, 042683033, 042683045, 042683058, 042683060, 042683072, 042683084 |
| JP | 医薬品医療機器総合機構 | 1190025F1023 |
| LT | Valstybinė vaistų kontrolės tarnyba | 1069509, 1069510, 1069511, 1069512, 1069513, 1071813 |
| NL | Z-Index G-Standaard, PRK | 106836 |
| PL | Rejestru Produktów Leczniczych | 100299622 |
| RO | Agenția Națională a Medicamentului și a Dispozitivelor Medicale | W59713001, W59713002, W59713003, W59713004, W59713005 |
| TR | İlaç ve Tıbbi Cihaz Kurumu | 8699795091021, 8699795091038, 8699795091045, 8699795091052 |
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