VESANOID

This brand name is authorized in Austria, Brazil, Canada, Croatia, Estonia, Finland, France, Hong Kong SAR China, Ireland, Israel, Japan, Malta, Mexico, Netherlands, New Zealand, Poland, Romania, Singapore, South Africa, Spain, Turkey.

Active ingredients

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

1
UNII 5688UTC01R - TRETINOIN
 

Tretinoin decreases cohesiveness of follicular epithelial cells resulting in decreased microcomedone formation. Additionally, tretinoin stimulates mitotic activity and increased turnover of follicular epithelial cells, causing extrusion of the comedones.

 
Read more about Tretinoin

Medicine classification

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

ATC Group Classification
L01XF01 Tretinoin L Antineoplastic and immunomodulating agents → L01 Antineoplastic agents → L01X Other antineoplastic agents → L01XF Retinoids for cancer treatment
Discover more medicines within L01XF01

Authorization and marketing

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

Country Identification scheme Identifier(s)
BR Câmara de Regulação do Mercado de Medicamentos 509018040022017
CA Health Products and Food Branch 02145839
EE Ravimiamet 1099087, 1668337
ES Centro de información online de medicamentos de la AEMPS 65396
FI Lääkealan turvallisuus- ja kehittämiskeskus 579417
FR Base de données publique des médicaments 65540866
HK Department of Health Drug Office 40621
HR Agencija za lijekove i medicinske proizvode HR-H-478293042
IL מִשְׂרַד הַבְּרִיאוּת 7344
JP 医薬品医療機器総合機構 4291006M1034
MT Medicines Authority AA565/64301, AA565/64303
MX Comisión Federal para la Protección contra Riesgos Sanitarios 546M96
NL Z-Index G-Standaard, PRK 45837
NZ Medicines and Medical Devices Safety Authority 7017
PL Rejestru Produktów Leczniczych 100070339
RO Agenția Națională a Medicamentului și a Dispozitivelor Medicale W67916001
SG Health Sciences Authority 08057P
TR İlaç ve Tıbbi Cihaz Kurumu 8680979254011
ZA Health Products Regulatory Authority 29/26/0087

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