AKLIEF

This brand name is authorized in Canada, Estonia, Spain, Finland, France, Hong Kong, Ireland, Malta, Netherlands, Poland, Romania, United States

Active ingredients

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

1 Trifarotene
UNII 0J8RN2W0HK - TRIFAROTENE

Trifarotene is an agonist of retinoic acid receptors (RAR), with particular activity at the gamma subtype of RAR. Stimulation of RAR results in modulation of target genes which are associated with various processes, including cell differentiation and mediation of inflammation. Trifarotene cream is used for the topical treatment of acne vulgaris.

Read about Trifarotene

Medication package inserts

Below package inserts are available for further reading:

Title Information Source Document Type  
AKLIEF Cream FDA, National Drug Code (US) MPI, US: SPL/PLR

Medicine classification

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

ATC code Group title Classification
D10AD06 D Dermatologicals → D10 Anti-acne preparations → D10A Anti-acne preparations for topical use → D10AD Retinoids for topical use in acne
Discover more medicines within D10AD06

Authorization and marketing

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

Country Identification scheme Identifier(s)
Country: CA Health Products and Food Branch Identifier(s): 02494175
Country: EE Ravimiamet Identifier(s): 1848843, 1848865, 1848876, 1848887
Country: ES Centro de información online de medicamentos de la AEMPS Identifier(s): 85017
Country: FI Lääkealan turvallisuus- ja kehittämiskeskus Identifier(s): 515832
Country: FR Base de données publique des médicaments Identifier(s): 63631908
Country: HK Department of Health Drug Office Identifier(s): 67256
Country: MT Medicines Authority Identifier(s): MA117/01501
Country: NL Z-Index G-Standaard, PRK Identifier(s): 203785
Country: PL Rejestru Produktów Leczniczych Identifier(s): 100412716
Country: RO Agenția Națională a Medicamentului și a Dispozitivelor Medicale Identifier(s): W68352001, W68352002, W68352003, W68352004
Country: US FDA, National Drug Code Identifier(s): 0299-5935

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