CUPRIOR

This brand name is authorized in Austria, Estonia, Finland, France, Croatia, Ireland, Lithuania, Netherlands, New Zealand, Poland, Romania, United Kingdom

Active ingredients

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

1 Trientine UNII 7360URE56Q - TRIENTINE TETRAHYDROCHLORIDE

Trientine is a copper-chelating agent whose principal mechanism of action is to eliminate absorbed copper from the body by forming a stable complex that is then eliminated through urinary excretion. Trientine may also chelate copper in the intestinal tract and so inhibit copper absorption. Read about Trientine

Medication package inserts

Below package inserts are available for further reading:

Title	Information Source	Document Type
CUPRIOR Film-coated tablet	European Medicines Agency (EU)	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
A16AX12		A Alimentary tract and metabolism → A16 Other alimentary tract and metabolism products → A16A Other alimentary tract and metabolism products → A16AX Various alimentary tract and metabolism products
Discover more medicines within A16AX12

Authorization and marketing

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

Country	Identification scheme	Identifier(s)
Country: EE	Ravimiamet	Identifier(s): 1752959, 1829594
Country: FI	Lääkealan turvallisuus- ja kehittämiskeskus	Identifier(s): 523961
Country: FR	Base de données publique des médicaments	Identifier(s): 66671295
Country: GB	Medicines & Healthcare Products Regulatory Agency	Identifier(s): 370820
Country: IE	Health Products Regulatory Authority	Identifier(s): 89008
Country: LT	Valstybinė vaistų kontrolės tarnyba	Identifier(s): 1083793, 1088644
Country: NL	Z-Index G-Standaard, PRK	Identifier(s): 197572
Country: NZ	Medicines and Medical Devices Safety Authority	Identifier(s): 20930
Country: PL	Rejestru Produktów Leczniczych	Identifier(s): 100400334
Country: RO	Agenția Națională a Medicamentului și a Dispozitivelor Medicale	Identifier(s): W68892001