CLOBEX

This brand name is authorized in United States. It is also authorized in Australia, Austria, Canada, Finland, France, Hong Kong SAR China, Netherlands, New Zealand, Poland, Singapore, South Africa, Spain, Tunisia.

Active ingredients

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

1
UNII 779619577M - CLOBETASOL PROPIONATE
 

Clobetasol propionate, like other topical corticosteroids, has anti-inflammatory, antipruritic, and vasoconstrictive properties. Corticosteroids are thought to act by the induction of phospholipase A2 inhibitory proteins, collectively called lipocortins. It is postulated that these proteins control the biosynthesis of potent mediators of inflammation such as prostaglandins and leukotrienes by inhibiting the release of their common precursor arachidonic acid.

 
Read more about Clobetasol propionate

Medicine classification

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

ATC Group Classification
D07AD01 Clobetasol D Dermatologicals → D07 Corticosteroids, dermatological preparations → D07A Corticosteroids, plain → D07AD Corticosteroids, very potent (group IV)
Discover more medicines within D07AD01

Authorization and marketing

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

Country Identification scheme Identifier(s)
AU Pharmaceutical Benefits Scheme 10080M
CA Health Products and Food Branch 02256371, 02299739
ES Centro de información online de medicamentos de la AEMPS 68316
FI Lääkealan turvallisuus- ja kehittämiskeskus 066578
FR Base de données publique des médicaments 61312395, 66815710, 68990516, 69724301
HK Department of Health Drug Office 53048, 64447
NL Z-Index G-Standaard, PRK 84069
NZ Medicines and Medical Devices Safety Authority 12183
PL Rejestru Produktów Leczniczych 100175400, 100467089
SG Health Sciences Authority 13239P, 13291P, 15185P
TN Direction de la Pharmacie et du Médicament 7393081
US FDA, National Drug Code 0299-3847, 0299-3848, 0299-3849
ZA Health Products Regulatory Authority 46/13.4.1/0556, A40/13.4.1/0035

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