ZANOSAR

This brand name is authorized in United States. It is also authorized in Estonia, Finland, Japan, UK.

Active ingredients

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

1
UNII 5W494URQ81 - STREPTOZOCIN
 
Read more about Streptozocin

Medication package inserts

Below package inserts are available for further reading:

Document Type Information Source  
 ZANOSAR Powder for concentrate for solution MPI, EU: SmPC Medicines & Healthcare Products Regulatory Agency (GB)

Medicine classification

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

ATC Group Classification
L01AD04 Streptozocin L Antineoplastic and immunomodulating agents → L01 Antineoplastic agents → L01A Alkylating agents → L01AD Nitrosoureas
Discover more medicines within L01AD04

Authorization and marketing

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

Country Identification scheme Identifier(s)
EE Ravimiamet 1778250, 1778531
FI Lääkealan turvallisuus- ja kehittämiskeskus 399347
GB Medicines & Healthcare Products Regulatory Agency 356918
JP 医薬品医療機器総合機構 4219406D1026
US FDA, National Drug Code 0703-4636

© All content on this website, including data entry, data processing, decision support tools, "RxReasoner" logo and graphics, is the intellectual property of RxReasoner and is protected by copyright laws. Unauthorized reproduction or distribution of any part of this content without explicit written permission from RxReasoner is strictly prohibited. Any third-party content used on this site is acknowledged and utilized under fair use principles.