CONDYLINE

This brand name is authorized in Canada, Estonia, France, Ireland, Netherlands, New Zealand, Poland, Romania, United Kingdom

Active ingredients

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

1 Podophyllotoxin
UNII L36H50F353 - PODOFILOX

Podophyllotoxin is a metaphase inhibitor in dividing cells binding to at least one binding site on tubulin. Binding prevents tubulin polymerisation required for microtubule assembly. At higher concentrations, podophyllotoxin also inhibits nucleoside transport through the cell membrane.

Read about Podophyllotoxin

Medication package inserts

Below package inserts are available for further reading:

Title Information Source Document Type  
CONDYLINE Cutaneous solution Medicines & Healthcare Products Regulatory Agency (GB) 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
D06BB04 Podophyllotoxin D Dermatologicals → D06 Antibiotics and chemotherapeutics for dermatological use → D06B Chemotherapeutics for topical use → D06BB Antivirals
Discover more medicines within D06BB04

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): 01945149
Country: EE Ravimiamet Identifier(s): 1813812, 1831531
Country: FR Base de données publique des médicaments Identifier(s): 61111385
Country: GB Medicines & Healthcare Products Regulatory Agency Identifier(s): 38491
Country: IE Health Products Regulatory Authority Identifier(s): 13209
Country: NL Z-Index G-Standaard Identifier(s): 13184946
Country: NL Z-Index G-Standaard, PRK Identifier(s): 72419
Country: NZ Medicines and Medical Devices Safety Authority Identifier(s): 5378
Country: PL Rejestru Produktów Leczniczych Identifier(s): 100015620, 100355071, 100358721, 100369825, 100437188
Country: RO Agenția Națională a Medicamentului și a Dispozitivelor Medicale Identifier(s): W66142001

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