TARGRETIN

This brand name is authorized in United States. It is also authorized in Austria, Croatia, Estonia, Finland, France, Ireland, Italy, Japan, Lithuania, Netherlands, Poland, Romania, Spain, UK.

Active ingredients

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

1
UNII A61RXM4375 - BEXAROTENE
 

Bexarotene is a synthetic compound that exerts its biological action through selective binding and activation of the three RXRs: α, β, and γ. Once activated, these receptors function as transcription factors that regulate processes such as cellular differentiation and proliferation, apoptosis, and insulin sensitisation. The exact mechanism of action of bexarotene in the treatment of cutaneous T-cell lymphoma (CTCL) is unknown.

 
Read more about Bexarotene

Medication package inserts

Below package inserts are available for further reading:

Document Type Information Source  
 Targretin Capsules MPI, EU: SmPC Medicines & Healthcare Products Regulatory Agency (GB)
 TARGRETIN Soft capsule MPI, EU: SmPC European Medicines Agency (EU)

Medicine classification

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

ATC Group Classification
L01XF03 Bexarotene L Antineoplastic and immunomodulating agents → L01 Antineoplastic agents → L01X Other antineoplastic agents → L01XF Retinoids for cancer treatment
Discover more medicines within L01XF03

Authorization and marketing

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

Country Identification scheme Identifier(s)
EE Ravimiamet 1196984
ES Centro de información online de medicamentos de la AEMPS 01178001
FI Lääkealan turvallisuus- ja kehittämiskeskus 431604
FR Base de données publique des médicaments 69197468
GB Medicines & Healthcare Products Regulatory Agency 43294
IE Health Products Regulatory Authority 88403
IT Agenzia del Farmaco 035710019
JP 医薬品医療機器総合機構 4291042M1022
LT Valstybinė vaistų kontrolės tarnyba 1031005
NL Z-Index G-Standaard, PRK 70610
PL Rejestru Produktów Leczniczych 100133583
RO Agenția Națională a Medicamentului și a Dispozitivelor Medicale W66654001
US FDA, National Drug Code 0187-5525, 0187-5526

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