This brand name is authorized in Austria, Croatia, Estonia, Ireland, Poland.
The drug CUPRYMINA contains one active pharmaceutical ingredient (API):
1
|
UNII
3IGV2Y2378 - CUPRIC CHLORIDE ANHYDROUS CU-64
|
Copper-64 chloride is a radiopharmaceutical precursor. It is not intended for direct use in patients. This medicinal product must be used only for the radiolabelling of carrier molecules, which have been specifically developed and authorised for radiolabelling with this radionuclide. |
|
Below package inserts are available for further reading:
Document | Type | Information Source | |
---|---|---|---|
CUPRYMINA Radiopharmaceutical precursor, solution | MPI, EU: SmPC | European Medicines Agency (EU) |
This drug has been classified in the anatomical therapeutic chemical (ATC) classification system as follows:
ATC Group | Classification | |
---|---|---|
V09XX | Various diagnostic radiopharmaceuticals | V Various → V09 Diagnostic radiopharmaceuticals → V09X Other diagnostic radiopharmaceuticals |
This drug has been assigned below unique identifiers within the countries it is being marketed:
Country | Identification scheme | Identifier(s) |
---|---|---|
EE | Ravimiamet | 1592984 |
PL | Rejestru Produktów Leczniczych | 100309349 |
© 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.