This brand name is authorized in Australia, Austria, Croatia, Cyprus, Estonia, France, Germany, Hong Kong SAR China, Ireland, Israel, Italy, Lithuania, Mexico, Poland, Romania, Singapore, South Africa, Spain, Tunisia, Turkey, UK.
The drug SOLIAN contains one active pharmaceutical ingredient (API):
1
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UNII
8110R61I4U - AMISULPRIDE
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Amisulpride is a neuroleptic. Amisulpride binds selectively with a high affinity to human dopaminergic D2/D3 receptor subtypes whereas it is devoid of affinity for D1, D4 and D5 receptor subtypes. |
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Below package inserts are available for further reading:
| Document | Type | Information Source | |
|---|---|---|---|
| SOLIAN Tablets | 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 | |
|---|---|---|
| N05AL05 | Amisulpride | N Nervous system → N05 Psycholeptics → N05A Antipsychotics → N05AL Benzamides |
This drug has been assigned below unique identifiers within the countries it is being marketed:
| Country | Identification scheme | Identifier(s) |
|---|---|---|
| AU | Pharmaceutical Benefits Scheme | 8594H, 8595J, 8596K, 8736T |
| DE | Bundesinstitut für Arzneimittel und Medizinprodukte | 00018431, 01827397, 01827434, 01827440, 02246917, 06136433, 08425012, 08425029 |
| EE | Ravimiamet | 1012105, 1041141, 1067497 |
| ES | Centro de información online de medicamentos de la AEMPS | 5267, 63994, 63995, 63996, 65991 |
| FR | Base de données publique des médicaments | 60019927, 62921036, 63697872, 64726693, 65637856 |
| GB | Medicines & Healthcare Products Regulatory Agency | 143684, 143691, 143697, 19246, 19247, 19250, 28422, 39342 |
| HK | Department of Health Drug Office | 46025, 47779, 47780 |
| HR | Agencija za lijekove i medicinske proizvode | HR-H-345193647 |
| IE | Health Products Regulatory Authority | 46655, 46708, 46724, 46857, 46870, 62895, 62897 |
| IL | מִשְׂרַד הַבְּרִיאוּת | 4588, 4589 |
| IT | Agenzia del Farmaco | 033462021, 033462045 |
| LT | Valstybinė vaistų kontrolės tarnyba | 1003162, 1003618, 1012368, 1067873, 1087921 |
| MX | Comisión Federal para la Protección contra Riesgos Sanitarios | 580M2000 |
| PL | Rejestru Produktów Leczniczych | 100098237, 100098243, 100098266, 100375010, 100450297, 100458238, 100461179 |
| RO | Agenția Națională a Medicamentului și a Dispozitivelor Medicale | W64419001, W64420001 |
| SG | Health Sciences Authority | 09773P, 11463P, 11464P |
| TN | Direction de la Pharmacie et du Médicament | 6483104, 6483105 |
| TR | İlaç ve Tıbbi Cihaz Kurumu | 8699809018563, 8699809018570, 8699809097759, 8699809097766, 8699809655065 |
| ZA | Health Products Regulatory Authority | 34/2.6.5/0116, 34/2.6.5/0117 |
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