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Fenofibrate
Chemical Name | ：Fenofibrate |
Category | ： |
Specification | ：EP/BP/USP |
HS Code | ：29189900.90 |
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Structure Formula | ： |
CAS Number | ：49562-28-9 |
Molecular Formula | ：C20H21ClO4 |
Usage | ：This product has a significant function of lowering serum cholesterol under the effect of esterase rapidly metabolized in the body of fenofibrate acid and landing blood lipid and lowering triglyceride level and increase high density lipoprotein cholesterol. It is suitable for the treatment of high blood triglycerides and hypercholesterolemia, whose curative effect is superior to the chlorine Bert with less side effects. |
Items | Standard |
|---|---|
Appearance | White or slightly yellow, crystalline powder |
Solubility | Practically insoluble in water, freely soluble in anhydrous ethanol, soluble in toluene. |
Melting point | 116 – 118℃ |
Identification | IR: Should be identical to that of RS |
Appearance of solution | Clear, not more than BY4 |
Water | ≤0.5% |
Chlorides | ≤350ppm |
Sulphated ash | ≤0.1% |
Related substances | Impurity A≤0.1% Impurity B≤0.2% Impurity C≤0.1% Impurity D≤0.1% Impurity E≤0.8% Any other impurity ≤0.1% Total of other impurities ≤0.5% |
Assay | 99%-101%(anhydrous substance) |
Residual solvents | Toluene≤890ppm Hexane≤290ppm |
1， Argentinian National Institute of Drugs
Instituto Nacional de Medicamentos (INAME)
2， Australian Therapeutic Goods Administration (TGA)
3， Belgian Federal Agency for Medicines and Health Products
Agence Fédérale des Médicaments et des Produits de Santé(AFMPS)
Federaal Agentschap voor Geneesmiddelen enGezondheidsproducten (FAGG)
4， Canadian Health Products and Food Branch Inspectorate(HPFBI)
5， Taiwan Food and Drug Administration (TFDA)
7， Czech State Institute for Drug Control
Státní Ústav pro Kontrolu Léčiv (SÚKL)
8， Czech Institute for State Control of Veterinary Biologicals and Medicines (ISCVBM)
9， Danish Health and Medicines Authority (DHMA)
10， Finnish Medicines Agency (FIMEA)
11， French National Agency for Medicines and Health Products Safety
Agence nationale de sécurité du médicament et des produits de santé (ANSM)
12， French Agency for Food, Environmental & Occupational Health Safety
Agence nationale de sécurité sanitaire de l'alimentation, de l'environnement et du travail (ANSES)
13， German Federal Ministry of Health *
Bundesministerium für Gesundheit (BMG)
14， Icelandic Medicines Agency (IMA)
20， Indonesian National Agency for Drug and Food Control (NADFC)
21， Health Products Regulatory Authority (HPRA)
22， Italian Medicines Agency
Agenzia Italiana del Farmaco (AIFA)
23， Japanese Pharmaceuticals and Medical Devices Agency(PMDA)
24， Korea (Republic of) Ministry of Food and Drug Safety (MFDS)
25， Malaysian National Pharmaceutical Control Bureau (NPCB)
26， Dutch Health Care Inspectorate*
Inspectie voor de Gezondheidszorg (IGZ)
27， New Zealand's Medicines and Medical Devices Safety Authority (Medsafe)
28， Norwegian Medicines Agency (NOMA)
29， Polish Main Pharmaceutical Inspectorate (MPI)
30， Romanian National Agency for Medicines and MedicalDevices (NAMMD)
31， South African Medicines Control Council (MCC)
32， Spanish Agency of Medicines and Medical Devices *
Agencia Española de Medicamentos y Productos Sanitarios(AEMPS)
33， Swedish Medical Products Agency (MPA)
34， United Kingdom's Medicines and Healthcare Products Regulatory Agency (MHRA)
35， United Kingdom's Veterinary Medicine Directorate (VMD)
36， U.S. Food and Drug Administration (US FDA)
37， European Directorate for the Quality of Medicines & HealthCare （EDQM）
38， European Medicines Agency（EMA）
39， World Health Organization（WHO）