This brand name is authorized in Nigeria. It is also authorized in Australia, Austria, Brazil, Canada, Cyprus, Ecuador, France, Germany, Hong Kong SAR China, Ireland, Italy, Malta, Mexico, Netherlands, Poland, Singapore, South Africa, Spain, Tunisia, Turkey, UK.
The drug DIAMICRON contains one active pharmaceutical ingredient (API):
1
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UNII
G4PX8C4HKV - GLICLAZIDE
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Gliclazide is a hypoglycaemic sulfonylurea antidiabetic active substance. Gliclazide reduces blood glucose levels by stimulating insulin secretion from the β-cells of the islets of Langerhans. |
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This drug has been approved in Nigeria as follows:
| Identifier | Form | Presentation | Description | Approval |
|---|---|---|---|---|
| A4-7426 | Tablet | DIAMICRON MR 60MG TABLETS TAB 60 mg 2X15 packs | 85 RNW-PP-274114 DIAMICRON MR 60MG TABLETS GLICLAZIDE Gliclazide 60mg A4 - 7426 Drugs Imported Products 215packs Prescription Only Medicine (POM) 8/19/2022 SERVIER PHARMACEUTICALS DEVELOPMENT LIMITED, 18A, OLU HOLLOWAY ROAD, IKOYI LAGOS LAGOS Les Laboratoires Servier Industrie, 905,route de Saran -45520 Gidy, France, France | 27/03/2024 |
Below package inserts are available for further reading:
| Document | Type | Information Source | |
|---|---|---|---|
| DIAMICRON MR Modified release tablet | MPI, EU: SmPC | Health Products Regulatory Authority (IE) |
This drug has been classified in the anatomical therapeutic chemical (ATC) classification system as follows:
| ATC Group | Classification | |
|---|---|---|
| A10BB09 | Gliclazide | A Alimentary tract and metabolism → A10 Drugs used in diabetes → A10B Blood glucose lowering drugs, excl. insulins → A10BB Sulfonamides, urea derivatives |
This drug has been assigned below unique identifiers within the countries it is being marketed:
| Country | Identification scheme | Identifier(s) |
|---|---|---|
| AU | Pharmaceutical Benefits Scheme | 9302N |
| BR | Câmara de Regulação do Mercado de Medicamentos | 531300504111317, 531300602113314, 531300603111315, 531300604116310, 531300605112319 |
| CA | Health Products and Food Branch | 00765996, 02242987, 02356422 |
| DE | Bundesinstitut für Arzneimittel und Medizinprodukte | 06488698, 06488706 |
| EC | Agencia Nacional de Regulación, Control y Vigilancia Sanitaria | 29539-12-10, 29578-2-01-11 |
| ES | Centro de información online de medicamentos de la AEMPS | 63644, 71738 |
| FR | Base de données publique des médicaments | 60331738, 68419097, 68831670 |
| GB | Medicines & Healthcare Products Regulatory Agency | 138648, 143135, 14761, 161583, 36622, 36623 |
| HK | Department of Health Drug Office | 46779, 60658 |
| IE | Health Products Regulatory Authority | 46985, 69515, 69540 |
| IT | Agenzia del Farmaco | 023404092, 023404231, 045454016, 045630011, 045637016, 045637028 |
| MT | Medicines Authority | MA066/00601, MA066/00603, MA066/00604, PI1438/05001A, PI1438/05002A, PI521/07601A, PI770/10702A, PI770/10703A, PI908/00902A, PI908/00903A |
| MX | Comisión Federal para la Protección contra Riesgos Sanitarios | 022M2002 |
| NG | Registered Drug Product Database | A4-7426, B4-9083 |
| NL | Z-Index G-Standaard, PRK | 61530 |
| PL | Rejestru Produktów Leczniczych | 100135837 |
| SG | Health Sciences Authority | 04316P, 11761P, 13868P |
| TN | Direction de la Pharmacie et du Médicament | 6350013, 9163581, 9253881, 9253882 |
| TR | İlaç ve Tıbbi Cihaz Kurumu | 8699552030058, 8699552030065, 8699552030072, 8699552030089, 8699552030096 |
| ZA | Health Products Regulatory Authority | 35/21.2/0178, 43/21.2/0957 |
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