BELKYRA

This brand name is authorized in Austria, Brazil, Canada, Estonia, Spain, Finland, Hong Kong, Ireland, Lithuania, Malta, New Zealand, Poland, Romania, Singapore, United Kingdom

Active ingredients

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

1 Deoxycholic acid
UNII 005990WHZZ - DEOXYCHOLIC ACID

Deoxycholic acid is a cytolytic drug, which when injected into localized subcutaneous fat, physically disrupts the cell membrane of adipocytes. The destruction of adipocytes elicits a tissue response in which macrophages are attracted to the area to eliminate cellular debris and lipids, which are then cleared through natural processes.

Read about Deoxycholic acid

Medication package inserts

Below package inserts are available for further reading:

Title Information Source Document Type  
BELKYRA Solution for injection Health Products Regulatory Authority (IE) MPI, EU: SmPC

Medicine classification

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

ATC code Group title Classification
D11AX24 D Dermatologicals → D11 Other dermatological preparations → D11A Other dermatological preparations → D11AX Other dermatologicals
Discover more medicines within D11AX24

Authorization and marketing

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

Country Identification scheme Identifier(s)
Country: BR Câmara de Regulação do Mercado de Medicamentos Identifier(s): 501019070014202
Country: CA Health Products and Food Branch Identifier(s): 02443910
Country: EE Ravimiamet Identifier(s): 1694077
Country: ES Centro de información online de medicamentos de la AEMPS Identifier(s): 81627
Country: FI Lääkealan turvallisuus- ja kehittämiskeskus Identifier(s): 476387
Country: GB Medicines & Healthcare Products Regulatory Agency Identifier(s): 383805
Country: HK Department of Health Drug Office Identifier(s): 65660
Country: LT Valstybinė vaistų kontrolės tarnyba Identifier(s): 1077740
Country: MT Medicines Authority Identifier(s): MA1304/00501
Country: NZ Medicines and Medical Devices Safety Authority Identifier(s): 18743
Country: PL Rejestru Produktów Leczniczych Identifier(s): 100352517
Country: RO Agenția Națională a Medicamentului și a Dispozitivelor Medicale Identifier(s): W69267001
Country: SG Health Sciences Authority Identifier(s): 15509P

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