PROCYSBI

This brand name is authorized in United States. It is also authorized in Austria, Canada, Croatia, Estonia, Finland, France, Ireland, Italy, Lithuania, Poland, Romania, Spain, UK.

Active ingredients

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

1
UNII QO84GZ3TST - CYSTEAMINE BITARTRATE
 

Mercaptamine reduces corneal cystine crystal accumulation acting as a cystine-depleting agent by converting cystine to cysteine and cysteine-cysteamine mixed disulfides.

 
Read more about Mercaptamine

Medication package inserts

Below package inserts are available for further reading:

Document Type Information Source  
 PROCYSBI Capsule / Granules MPI, US: SPL/PLR FDA, National Drug Code (US)

Medicine classification

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

ATC Group Classification
A16AA04 Mercaptamine A Alimentary tract and metabolism → A16 Other alimentary tract and metabolism products → A16A Other alimentary tract and metabolism products → A16AA Amino acids and derivatives
Discover more medicines within A16AA04

Authorization and marketing

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

Country Identification scheme Identifier(s)
CA Health Products and Food Branch 02464705, 02464713
EE Ravimiamet 1624845, 1624856
ES Centro de información online de medicamentos de la AEMPS 113861001, 113861002
FI Lääkealan turvallisuus- ja kehittämiskeskus 436647, 494885
FR Base de données publique des médicaments 65249056, 69022853
GB Medicines & Healthcare Products Regulatory Agency 307180, 307186
IE Health Products Regulatory Authority 88990, 88991
IT Agenzia del Farmaco 043041019, 043041021, 043041033, 043041045
LT Valstybinė vaistų kontrolės tarnyba 1071193, 1071194
PL Rejestru Produktów Leczniczych 100313291, 100313300
RO Agenția Națională a Medicamentului și a Dispozitivelor Medicale W66425001, W66426001
US FDA, National Drug Code 75987-100, 75987-101, 75987-140, 75987-145

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