LOPID

This brand name is authorized in United States. It is also authorized in Ecuador, Finland, Hong Kong SAR China, Ireland, Italy, Mexico, Netherlands, South Africa, Spain, Turkey, UK.

Active ingredients

The drug LOPID contains one active pharmaceutical ingredient (API):

1
UNII Q8X02027X3 - GEMFIBROZIL
 

Gemfibrozil is a lipid regulating agent which regulates lipid fractions. Gemfibrozil stimulates the peripheral lipolysis of triglyceride rich lipoproteins such as VLDL and cholymicrons by stimulation of LPL. Gemfibrozil also inhibits synthesis of VLDL in the liver.

 
Read more about Gemfibrozil

Medication package inserts

Below package inserts are available for further reading:

Document Type Information Source  
 LOPID Film-coated tablet MPI, EU: SmPC Medicines & Healthcare Products Regulatory Agency (GB)

Medicine classification

This drug has been classified in the anatomical therapeutic chemical (ATC) classification system as follows:

ATC Group Classification
C10AB04 Gemfibrozil C Cardiovascular system → C10 Lipid modifying agents → C10A Lipid modifying agents, plain → C10AB Fibrates
Discover more medicines within C10AB04

Authorization and marketing

This drug has been assigned below unique identifiers within the countries it is being marketed:

Country Identification scheme Identifier(s)
EC Agencia Nacional de Regulación, Control y Vigilancia Sanitaria 30038-11-11, 30046-11-11, 363311112
ES Centro de información online de medicamentos de la AEMPS 58832, 61026
FI Lääkealan turvallisuus- ja kehittämiskeskus 469346
GB Medicines & Healthcare Products Regulatory Agency 13916, 143316, 162007, 209799, 373779
HK Department of Health Drug Office 30985
IE Health Products Regulatory Authority 31941, 32150, 54369
IT Agenzia del Farmaco 025445026, 025445053
MX Comisión Federal para la Protección contra Riesgos Sanitarios 107M84
NL Z-Index G-Standaard, PRK 31062
TR İlaç ve Tıbbi Cihaz Kurumu 8681308091222, 8681308091239
US FDA, National Drug Code 0071-0737
ZA Health Products Regulatory Authority Y/7.5/245

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