CLOPIXOL

This brand name is authorized in Australia, Brazil, Canada, Cyprus, France, Germany, Hong Kong SAR China, Ireland, Israel, Malta, Mexico, New Zealand, Poland, Romania, Singapore, South Africa, Spain, Turkey, UK.

Active ingredients

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

1
UNII 47ISU063SG - ZUCLOPENTHIXOL
 

Zuclopenthixol is a potent neuroleptic of the thioxanthene series with a piperazine side-chain. The antipsychotic effect of neuroleptics is related to their dopamine receptor blocking effect.

 
Read more about Zuclopenthixol

Medication package inserts

Below package inserts are available for further reading:

Document Type Information Source  
 CLOPIXOL Solution for injection MPI, EU: SmPC Medicines & Healthcare Products Regulatory Agency (GB)
 CLOPIXOL ACUPHASE Solution for injection MPI, EU: SmPC Medicines & Healthcare Products Regulatory Agency (GB)
 CLOPIXOL Film-coated tablet 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
N05AF05 Zuclopenthixol N Nervous system → N05 Psycholeptics → N05A Antipsychotics → N05AF Thioxanthene derivatives
Discover more medicines within N05AF05

Authorization and marketing

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

Country Identification scheme Identifier(s)
AU Pharmaceutical Benefits Scheme 8097E
BR Câmara de Regulação do Mercado de Medicamentos 524200201114412, 524200202110410, 524200203151412, 524200204156418
CA Health Products and Food Branch 02230402, 02230403, 02230405, 02230406
DE Bundesinstitut für Arzneimittel und Medizinprodukte 01125028, 01177930, 02522056, 02752543, 02752566, 03569634, 06585384, 06729469, 09102802, 09321792, 10930740, 13713552, 14136051, 14236605, 15266318, 17562908
ES Centro de información online de medicamentos de la AEMPS 60871, 60872, 60873, 60874, 60875
FR Base de données publique des médicaments 60209937, 61323662, 62788550, 63744998, 68072846, 69974746
GB Medicines & Healthcare Products Regulatory Agency 147150, 147160, 198691, 24633, 24634, 24635, 27619, 27629, 377428, 399365, 41302
HK Department of Health Drug Office 19861, 22761
IE Health Products Regulatory Authority 17841, 17914, 18139
IL מִשְׂרַד הַבְּרִיאוּת 2426, 623, 624, 626, 627, 628, 629, 630, 6787, 6788, 6789, 6790
MT Medicines Authority AA565/28903, MA1323/00101
MX Comisión Federal para la Protección contra Riesgos Sanitarios 414M96, 415M96, 417M96
NZ Medicines and Medical Devices Safety Authority 5434, 5435, 5436
PL Rejestru Produktów Leczniczych 100015033, 100015040, 100015056, 100248091
RO Agenția Națională a Medicamentului și a Dispozitivelor Medicale W10638002, W12431001, W12437002, W12437003, W12439002, W12439003, W13182005
SG Health Sciences Authority 01365P
TR İlaç ve Tıbbi Cihaz Kurumu 8699795090505, 8699795091335, 8699795091342, 8699795590012, 8699795750201, 8699795750225
ZA Health Products Regulatory Authority R/2.6.5/52, T/2.6.5/180, T/2.6.5/181, W/2.6.5/27

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