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01 12care4
02 3AAIPharma Services Corp.
03 2Actavis Nordic A/S
04 4Alphapharm PTY Ltd
05 4Arrotex Pharmaceuticals
06 2Bausch Health
07 2Ebb Medical
08 2F. Hoffmann-La Roche
09 3Meda - Asker
10 1Meda Ab
11 7ORIFARM GROUP AS
12 5Paranova Pharmaceuticals Ab
13 2Pharma Dynamics
14 2Pharmascience Inc.
15 5Ratiopharm GmbH
16 2STADA Arzneimittel
17 5Sandoz B2B
18 1Strides Pharma SA (Pty) Ltd
19 2Unimedic AB
20 11Viatris
21 4WAGNER PHARMACEUTICALS PTY LTD
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01 8Antic-calc Tablet, Film Coated
02 17Film Coated Tablet
03 6TAB
04 7TABLET
05 12Tablet
06 20tablet
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01 2Allowed
02 3Approved
03 2Authorized
04 22Deregistered
05 4Generic
06 2Originator
07 7Prescription
08 28Blank
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01 2Amira 150
02 2Amira 300
03 26Aurorix
04 2Aurorix 300 mg
05 4Clobemix
06 1Clorix 150
07 1Clorix 300
08 1Depnil
09 2MANERIX
10 3MOCLOBEMIDE
11 4MOCLOBEMIDE-WGR
12 2Manerix
13 1Medpro-Ciprofloxacin 750
14 5Moclobemid ratiopharm
15 2Moclobemide Actavis
16 2Moclobemide Alternova
17 4Moclobemide Sandoz
18 2Moclobemide Stada
19 2Moklobemid Mylan
20 2PMS-MOCLOBEMIDE
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01 20Australia
02 7Canada
03 8Norway
04 6South Africa
05 2Spain
06 25Sweden
07 2Switzerland
Regulatory Info : Deregistered
Registration Country : Sweden
Brand Name : Aurorix
Dosage Form : Film Coated Tablet
Dosage Strength : 150mg
Packaging :
Approval Date : 07/04/2020
Application Number : 20191129000072
Regulatory Info : Deregistered
Registration Country : Sweden
Regulatory Info : Approved
Registration Country : Sweden
Brand Name : Aurorix
Dosage Form : Film Coated Tablet
Dosage Strength : 150mg
Packaging :
Approval Date : 17/12/2019
Application Number : 20190814000069
Regulatory Info : Approved
Registration Country : Sweden
Regulatory Info : Approved
Registration Country : Sweden
Brand Name : Aurorix
Dosage Form : Film Coated Tablet
Dosage Strength : 150mg
Packaging :
Approval Date : 06/11/2019
Application Number : 20190814000045
Regulatory Info : Approved
Registration Country : Sweden
Regulatory Info : Deregistered
Registration Country : Sweden
Brand Name : Aurorix
Dosage Form : Tablet
Dosage Strength : 150mg
Packaging :
Approval Date : 10/03/2000
Application Number : 20000310000022
Regulatory Info : Deregistered
Registration Country : Sweden
Regulatory Info : Deregistered
Registration Country : Sweden
Brand Name : Aurorix
Dosage Form : Tablet
Dosage Strength : 150mg
Packaging :
Approval Date : 17/05/2002
Application Number : 20020517000328
Regulatory Info : Deregistered
Registration Country : Sweden
Regulatory Info : Deregistered
Registration Country : Sweden
Brand Name : Aurorix
Dosage Form : Tablet
Dosage Strength : 150mg
Packaging :
Approval Date : 16/06/2000
Application Number : 20000616000054
Regulatory Info : Deregistered
Registration Country : Sweden
Regulatory Info : Prescription
Registration Country : Canada
Brand Name : PMS-MOCLOBEMIDE
Dosage Form : TABLET
Dosage Strength : 300MG
Packaging :
Approval Date :
Application Number :
Regulatory Info : Prescription
Registration Country : Canada
Regulatory Info : Prescription
Registration Country : Canada
Brand Name : PMS-MOCLOBEMIDE
Dosage Form : TABLET
Dosage Strength : 150MG
Packaging : 100/500
Approval Date :
Application Number :
Regulatory Info : Prescription
Registration Country : Canada
Regulatory Info :
Registration Country : Norway
Brand Name : Moclobemid ratiopharm
Dosage Form : Antic-calc Tablet, Film Coated
Dosage Strength : 150 mg
Packaging : Blister
Approval Date :
Application Number :
Regulatory Info :
Registration Country : Norway
Regulatory Info :
Registration Country : Norway
Brand Name : Moclobemid ratiopharm
Dosage Form : Antic-calc Tablet, Film Coated
Dosage Strength : 150 mg
Packaging : Blister
Approval Date :
Application Number :
Regulatory Info :
Registration Country : Norway
Regulatory Info :
Registration Country : Norway
Brand Name : Moclobemid ratiopharm
Dosage Form : Antic-calc Tablet, Film Coated
Dosage Strength : 150 mg
Packaging : Blister, endose
Approval Date :
Application Number :
Regulatory Info :
Registration Country : Norway
Regulatory Info :
Registration Country : Norway
Brand Name : Moclobemid ratiopharm
Dosage Form : Antic-calc Tablet, Film Coated
Dosage Strength : 300 mg
Packaging : Blister
Approval Date :
Application Number :
Regulatory Info :
Registration Country : Norway
Regulatory Info :
Registration Country : Norway
Brand Name : Moclobemid ratiopharm
Dosage Form : Antic-calc Tablet, Film Coated
Dosage Strength : 300 mg
Packaging : Blister
Approval Date :
Application Number :
Regulatory Info :
Registration Country : Norway
Regulatory Info : Deregistered
Registration Country : Sweden
Brand Name : Aurorix
Dosage Form : Tablet
Dosage Strength : 150mg
Packaging :
Approval Date : 30/11/2001
Application Number : 20011130000055
Regulatory Info : Deregistered
Registration Country : Sweden
Regulatory Info : Approved
Registration Country : Sweden
Brand Name : Aurorix
Dosage Form : Film Coated Tablet
Dosage Strength : 150mg
Packaging :
Approval Date : 08/12/1989
Application Number : 19891208000118
Regulatory Info : Approved
Registration Country : Sweden
Regulatory Info :
Registration Country : Norway
Brand Name : Aurorix
Dosage Form : Antic-calc Tablet, Film Coated
Dosage Strength : 150 mg
Packaging : Blister
Approval Date :
Application Number :
Regulatory Info :
Registration Country : Norway
Portfolio PDF
Product Web Link
Virtual Booth
Digital Content
Website
Corporate PDF
Regulatory Info :
Registration Country : Norway
Brand Name : Aurorix
Dosage Form : Antic-calc Tablet, Film Coated
Dosage Strength : 150 mg
Packaging : Blister
Approval Date :
Application Number :
Regulatory Info :
Registration Country : Norway
Portfolio PDF
Product Web Link
Virtual Booth
Digital Content
Website
Corporate PDF
Regulatory Info :
Registration Country : Norway
Brand Name : Aurorix
Dosage Form : Antic-calc Tablet, Film Coated
Dosage Strength : 300 mg
Packaging : Blister
Approval Date :
Application Number :
Regulatory Info :
Registration Country : Norway
Portfolio PDF
Product Web Link
Virtual Booth
Digital Content
Website
Corporate PDF
Regulatory Info : Deregistered
Registration Country : Sweden
Brand Name : Aurorix
Dosage Form : Tablet
Dosage Strength : 150mg
Packaging :
Approval Date : 30/07/1999
Application Number : 19990730000051
Regulatory Info : Deregistered
Registration Country : Sweden
Portfolio PDF
Product Web Link
Virtual Booth
Digital Content
Website
Corporate PDF
Regulatory Info : Deregistered
Registration Country : Sweden
Brand Name : Aurorix
Dosage Form : Tablet
Dosage Strength : 150mg
Packaging :
Approval Date : 30/07/1999
Application Number : 19990730000075
Regulatory Info : Deregistered
Registration Country : Sweden
Portfolio PDF
Product Web Link
Virtual Booth
Digital Content
Website
Corporate PDF