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01 3Ebb Medical
02 26H. Lundbeck AS
03 3ORIFARM GROUP AS
04 2Paranova Pharmaceuticals Ab
05 1Pharmachim Ab
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01 3Antic-calc Tablet, Film Coated
02 1Droplets, resolution
03 17Film Coated Tablet
04 1INJ
05 1Injectable Solution
06 1Oral Drop
07 1Oral Drops
08 1Oral Solution
09 1SOLUTION
10 2TAB
11 2TABLET
12 1Zuclopentixolo 200Mg 1 Unit Parenteral Use Rp
13 3Blank
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01 4Allowed
02 7Approved
03 3Authorized
04 7Deregistered
05 3Originator
06 3Prescription
07 8Blank
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01 2CLOPIXOL
02 1CLOPIXOL ACUPHASE
03 12Cisordinol
04 17Clopixol
05 1Clopixol Tablets 10 mg
06 1Clopixol Acuphase 50 mg/ml
07 1Clopixol Tablets 2 mg
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01 3Canada
02 4Italy
03 4Norway
04 3South Africa
05 3Spain
06 14Sweden
07 4Switzerland
Regulatory Info : Approved
Registration Country : Sweden
Zuclopenthixol Dihydrochloride
Brand Name : Cisordinol
Dosage Form : Film Coated Tablet
Dosage Strength : 10mg
Packaging :
Approval Date : 22/11/2024
Application Number : 20240806000017
Regulatory Info : Approved
Registration Country : Sweden
Regulatory Info : Approved
Registration Country : Sweden
Zuclopenthixol Dihydrochloride
Brand Name : Cisordinol
Dosage Form : Film Coated Tablet
Dosage Strength : 2mg
Packaging :
Approval Date : 10/04/2025
Application Number : 20250116000102
Regulatory Info : Approved
Registration Country : Sweden
Regulatory Info : Approved
Registration Country : Sweden
Zuclopenthixol Dihydrochloride
Brand Name : Cisordinol
Dosage Form : Film Coated Tablet
Dosage Strength : 25mg
Packaging :
Approval Date : 22/11/2024
Application Number : 20240806000024
Regulatory Info : Approved
Registration Country : Sweden
Regulatory Info :
Registration Country : Italy
Zuclopenthixol Dihydrochloride
Brand Name : Clopixol
Dosage Form : Zuclopentixolo 200Mg 1 Unit Parenteral Use Rp
Dosage Strength : 1 vial IM 200 mg 1 ml sustained release
Packaging :
Approval Date :
Application Number :
Regulatory Info :
Registration Country : Italy
Regulatory Info :
Registration Country : Italy
Zuclopenthixol Dihydrochloride
Brand Name : Clopixol
Dosage Form :
Dosage Strength : Gtt Os 10 Ml 20 Mg/Ml
Packaging :
Approval Date :
Application Number :
Regulatory Info :
Registration Country : Italy
Regulatory Info :
Registration Country : Italy
Zuclopenthixol Dihydrochloride
Brand Name : Clopixol
Dosage Form :
Dosage Strength : 30 Cpr 10 Mg
Packaging :
Approval Date :
Application Number :
Regulatory Info :
Registration Country : Italy
Regulatory Info :
Registration Country : Italy
Zuclopenthixol Dihydrochloride
Brand Name : Clopixol
Dosage Form :
Dosage Strength : 20 Cpr 25 Mg
Packaging :
Approval Date :
Application Number :
Regulatory Info :
Registration Country : Italy
Regulatory Info :
Registration Country : Norway
Zuclopenthixol Dihydrochloride
Brand Name : Cisordinol
Dosage Form : Antic-calc Tablet, Film Coated
Dosage Strength : 10 mg
Packaging : Box
Approval Date :
Application Number :
Regulatory Info :
Registration Country : Norway
Regulatory Info :
Registration Country : Norway
Zuclopenthixol Dihydrochloride
Brand Name : Cisordinol
Dosage Form : Antic-calc Tablet, Film Coated
Dosage Strength : 2 mg
Packaging : Box
Approval Date :
Application Number :
Regulatory Info :
Registration Country : Norway
Regulatory Info :
Registration Country : Norway
Zuclopenthixol Dihydrochloride
Brand Name : Cisordinol
Dosage Form : Droplets, resolution
Dosage Strength : 20 mg/ml
Packaging : Bottle of glass
Approval Date :
Application Number :
Regulatory Info :
Registration Country : Norway
Regulatory Info :
Registration Country : Norway
Zuclopenthixol Dihydrochloride
Brand Name : Cisordinol
Dosage Form : Antic-calc Tablet, Film Coated
Dosage Strength : 25 mg
Packaging : Box
Approval Date :
Application Number :
Regulatory Info :
Registration Country : Norway
Regulatory Info : Allowed
Registration Country : Switzerland
Brand Name : Clopixol
Dosage Form : Film Coated Tablet
Dosage Strength : 2mg
Packaging :
Approval Date : 06/12/1982
Application Number : 44744
Regulatory Info : Allowed
Registration Country : Switzerland
Regulatory Info : Allowed
Registration Country : Switzerland
Brand Name : Clopixol
Dosage Form : Film Coated Tablet
Dosage Strength : 10mg
Packaging :
Approval Date : 06/12/1982
Application Number : 44744
Regulatory Info : Allowed
Registration Country : Switzerland
Regulatory Info : Allowed
Registration Country : Switzerland
Brand Name : Clopixol
Dosage Form : Film Coated Tablet
Dosage Strength : 25mg
Packaging :
Approval Date : 06/12/1982
Application Number : 44744
Regulatory Info : Allowed
Registration Country : Switzerland
Regulatory Info : Allowed
Registration Country : Switzerland
Brand Name : Clopixol
Dosage Form : Oral Solution
Dosage Strength : 20mg/ml
Packaging :
Approval Date : 06/12/1982
Application Number : 44747
Regulatory Info : Allowed
Registration Country : Switzerland
Regulatory Info : Approved
Registration Country : Sweden
Zuclopenthixol Dihydrochloride
Brand Name : Cisordinol
Dosage Form : Film Coated Tablet
Dosage Strength : 10mg
Packaging :
Approval Date : 03/09/1982
Application Number : 19820903000093
Regulatory Info : Approved
Registration Country : Sweden
Regulatory Info : Approved
Registration Country : Sweden
Zuclopenthixol Dihydrochloride
Brand Name : Cisordinol
Dosage Form : Film Coated Tablet
Dosage Strength : 2mg
Packaging :
Approval Date : 03/09/1982
Application Number : 19820903000086
Regulatory Info : Approved
Registration Country : Sweden
Regulatory Info : Approved
Registration Country : Sweden
Zuclopenthixol Dihydrochloride
Brand Name : Cisordinol
Dosage Form : Oral Drops
Dosage Strength : 20mg/ml
Packaging :
Approval Date : 03/09/1982
Application Number : 19820903000062
Regulatory Info : Approved
Registration Country : Sweden
Regulatory Info : Approved
Registration Country : Sweden
Zuclopenthixol Dihydrochloride
Brand Name : Cisordinol
Dosage Form : Film Coated Tablet
Dosage Strength : 25mg
Packaging :
Approval Date : 03/09/1982
Application Number : 19820903000109
Regulatory Info : Approved
Registration Country : Sweden
Regulatory Info : Deregistered
Registration Country : Sweden
Zuclopenthixol Dihydrochloride
Brand Name : Cisordinol
Dosage Form : Injectable Solution
Dosage Strength : 10mg/ml
Packaging :
Approval Date : 03/09/1982
Application Number : 19820903000079
Regulatory Info : Deregistered
Registration Country : Sweden