CANCIDAS

This brand name is authorized in United States. It is also authorized in Austria, Brazil, Canada, Cyprus, Ecuador, Estonia, Finland, Ireland, Japan, Lithuania, Mexico, Netherlands, Nigeria, Poland, Romania, Singapore, South Africa, Spain, Tunisia, Turkey, UK.

Active ingredients

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

1
UNII VUW370O5QE - CASPOFUNGIN ACETATE
 

Caspofungin acetate is a semi-synthetic lipopeptide (echinocandin) compound synthesised from a fermentation product of Glarea lozoyensis. Caspofungin acetate inhibits the synthesis of beta (1,3)-D-glucan, an essential component of the cell wall of many filamentous fungi and yeast. Beta (1,3)-D-glucan is not present in mammalian cells.

 
Read more about Caspofungin

Medication package inserts

Below package inserts are available for further reading:

Document Type Information Source  
 CANCIDAS Powder for solution for infusion MPI, EU: SmPC European Medicines Agency (EU)

Medicine classification

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

ATC Group Classification
J02AX04 Caspofungin J Antiinfectives for systemic use → J02 Antimycotics for systemic use → J02A Antimycotics for systemic use → J02AX Other antimycotics for systemic use
Discover more medicines within J02AX04

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 525500301155311, 525500302151318
CA Health Products and Food Branch 02244265, 02244266
EC Agencia Nacional de Regulación, Control y Vigilancia Sanitaria 30028-11-11, 30033-11-11
EE Ravimiamet 1087477, 1092169
ES Centro de información online de medicamentos de la AEMPS 01196001, 01196003
FI Lääkealan turvallisuus- ja kehittämiskeskus 006079, 006115
GB Medicines & Healthcare Products Regulatory Agency 48475
JP 医薬品医療機器総合機構 6179402D1020, 6179402D2026
LT Valstybinė vaistų kontrolės tarnyba 1007521, 1028063
MX Comisión Federal para la Protección contra Riesgos Sanitarios 555M2000
NG Registered Drug Product Database B4-9092, B4-9093
NL Z-Index G-Standaard, PRK 70300, 70319
PL Rejestru Produktów Leczniczych 100126880, 100126896
RO Agenția Națională a Medicamentului și a Dispozitivelor Medicale W64792001, W64793001
SG Health Sciences Authority 11762P, 11763P
TN Direction de la Pharmacie et du Médicament 7013131H, 7013132H
TR İlaç ve Tıbbi Cihaz Kurumu 8699636260203, 8699636260227
US FDA, National Drug Code 0006-3822, 0006-3823
ZA Health Products Regulatory Authority 37/20.2.2/0544, 37/20.2.2/0545

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