KENALOG

This brand name is authorized in United States. It is also authorized in Canada, Croatia, Estonia, Lithuania, Malta, New Zealand, UK.

Active ingredients

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

1
UNII F446C597KA - TRIAMCINOLONE ACETONIDE
 

Triamcinolone acetonide is a more potent derivative of triamcinolone and is approximately 8 times more potent than prednisone. Although the precise mechanism of corticosteroid anti-allergic action is unknown, corticosteroids are very effective in the treatment of allergic diseases in man. Also, local injections are thought to have an anti-inflammatory effect.

 
Read more about Triamcinolone

Medication package inserts

Below package inserts are available for further reading:

Document Type Information Source  
 KENALOG-10 MPI, US: SPL/Old FDA, National Drug Code (US)

Medicine classification

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

ATC Group Classification
H02AB08 Triamcinolone H Systemic hormonal preparations, excl. Sex hormones and insulins → H02 Corticosteroids for systemic use → H02A CORTICOSTEROIDS FOR SYSTEMIC USE, PLAIN → H02AB Glucocorticoids
Discover more medicines within H02AB08

Authorization and marketing

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

Country Identification scheme Identifier(s)
CA Health Products and Food Branch 01999761, 01999869
EE Ravimiamet 1008425
GB Medicines & Healthcare Products Regulatory Agency 27559
HR Agencija za lijekove i medicinske proizvode HR-H-363427938
LT Valstybinė vaistų kontrolės tarnyba 1013970
MT Medicines Authority AA770/12401
NZ Medicines and Medical Devices Safety Authority 113
US FDA, National Drug Code 0003-0293, 0003-0315, 0003-0494, 10631-093, 50090-0256, 50090-0295, 50090-0819, 63187-661, 70518-2460, 76420-085

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