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01 1Allergan Aesthetics
02 1Aspen Pharmacare Holdings
03 2Aurobindo Pharma Limited
04 2Aurovitas Spain, Sau
05 1Bial
06 1Ivax Scandinavia Ab
07 1JAMP PHARMA
08 2Karo Pharma
09 1Medreich
10 1National Pharma
11 3ORIFARM GROUP AS
12 1Paranova Pharmaceuticals Ab
13 1Pharma Dynamics
14 1Pharmascience Inc.
15 1Sandoz B2B
16 3Teva Pharmaceutical Industries
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01 2Bezafibrate 400Mg 30 Joined' Oral Use Rp
02 2Extended-Release Tablet
03 3Film Coated Tablet
04 1Modified Release Tablet
05 1SRT
06 1Sustained Release Tablet
07 4TAB
08 1TABLET
09 2TABLET (EXTENDED-RELEASE)
10 6Tablet
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01 1Allowed
02 2Approved
03 2Authorized
04 1Cancelled
05 5Deregistered
06 3Generic
07 2Originator
08 3Prescription
09 4Blank
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01 1BEZALIP SR
02 1Bezachole Sr
03 1Bezafibrate
04 4Bezalip
05 6Bezalip Retard
06 1Cedur retard
07 1Difaterol Retard
08 1Dyna Bezafibrate Sr 400
09 1Eulitop
10 1Eulitop Retard
11 1JAMP-BEZAFIBRATE SR
12 1PMS-BEZAFIBRATE
13 1Sandoz Bezafibrate 400
14 2Blank
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01 3Canada
02 2India
03 2Italy
04 5South Africa
05 3Spain
06 7Sweden
07 1Switzerland
Regulatory Info : Prescription
Registration Country : Canada
Brand Name : BEZALIP SR
Dosage Form : TABLET (EXTENDED-RELEASE)
Dosage Strength : 400MG
Packaging : 30
Approval Date :
Application Number : 2083523
Regulatory Info : Prescription
Registration Country : Canada
Regulatory Info : Generic
Registration Country : South Africa
Brand Name : Bezachole Sr
Dosage Form : TAB
Dosage Strength : 400mg
Packaging : 30X1mg
Approval Date :
Application Number :
Regulatory Info : Generic
Registration Country : South Africa
Regulatory Info :
Registration Country : Italy
Brand Name : Bezafibrate
Dosage Form : Bezafibrate 400Mg 30 Joined' Oral Use Rp
Dosage Strength : 30 cpr riv 400 mg prolonged release
Packaging :
Approval Date :
Application Number :
Regulatory Info :
Registration Country : Italy
Regulatory Info :
Registration Country : Italy
Brand Name : Bezalip
Dosage Form : Bezafibrate 400Mg 30 Joined' Oral Use Rp
Dosage Strength : 30 cpr riv 400 mg prolonged release
Packaging :
Approval Date :
Application Number :
Regulatory Info :
Registration Country : Italy
Regulatory Info : Prescription
Registration Country : Canada
Brand Name : JAMP-BEZAFIBRATE SR
Dosage Form : TABLET (EXTENDED-RELEASE)
Dosage Strength : 400MG
Packaging : 30/100
Approval Date :
Application Number : 2453312
Regulatory Info : Prescription
Registration Country : Canada
Regulatory Info : Approved
Registration Country : Sweden
Brand Name : Bezalip
Dosage Form : Film Coated Tablet
Dosage Strength : 200mg
Packaging :
Approval Date : 28/09/1990
Application Number : 19900928000015
Regulatory Info : Approved
Registration Country : Sweden
Regulatory Info : Approved
Registration Country : Sweden
Brand Name : Bezalip Retard
Dosage Form : Tablet
Dosage Strength : 400mg
Packaging :
Approval Date : 29/06/1994
Application Number : 19940629000013
Regulatory Info : Approved
Registration Country : Sweden
Regulatory Info :
Registration Country : India
Brand Name :
Dosage Form : Sustained Release Tablet
Dosage Strength : 400MG
Packaging :
Approval Date :
Application Number :
Regulatory Info :
Registration Country : India
Regulatory Info :
Registration Country : India
Brand Name :
Dosage Form : Tablet
Dosage Strength : 40MG
Packaging :
Approval Date :
Application Number :
Regulatory Info :
Registration Country : India
Regulatory Info : Deregistered
Registration Country : Sweden
Brand Name : Bezalip
Dosage Form : Film Coated Tablet
Dosage Strength : 200mg
Packaging :
Approval Date : 19/10/2001
Application Number : 20011019000022
Regulatory Info : Deregistered
Registration Country : Sweden
Regulatory Info : Deregistered
Registration Country : Sweden
Brand Name : Bezalip Retard
Dosage Form : Tablet
Dosage Strength : 400mg
Packaging :
Approval Date : 11/02/2000
Application Number : 20000211000312
Regulatory Info : Deregistered
Registration Country : Sweden
Regulatory Info : Deregistered
Registration Country : Sweden
Brand Name : Bezalip Retard
Dosage Form : Tablet
Dosage Strength : 400mg
Packaging :
Approval Date : 24/09/1999
Application Number : 19990924000096
Regulatory Info : Deregistered
Registration Country : Sweden
Regulatory Info : Generic
Registration Country : South Africa
Brand Name : Dyna Bezafibrate Sr 400
Dosage Form : SRT
Dosage Strength : 400mg
Packaging : 30X1mg
Approval Date :
Application Number :
Regulatory Info : Generic
Registration Country : South Africa
Regulatory Info : Prescription
Registration Country : Canada
Brand Name : PMS-BEZAFIBRATE
Dosage Form : TABLET
Dosage Strength : 200MG
Packaging : 30/100
Approval Date :
Application Number :
Regulatory Info : Prescription
Registration Country : Canada
Regulatory Info : Generic
Registration Country : South Africa
Brand Name : Sandoz Bezafibrate 400
Dosage Form : TAB
Dosage Strength : 400mg
Packaging : 30X1mg
Approval Date :
Application Number :
Regulatory Info : Generic
Registration Country : South Africa
Regulatory Info : Allowed
Registration Country : Switzerland
Brand Name : Cedur retard
Dosage Form : Modified Release Tablet
Dosage Strength : 400mg
Packaging :
Approval Date : 22/04/1983
Application Number : 45352
Regulatory Info : Allowed
Registration Country : Switzerland
Regulatory Info : Originator
Registration Country : South Africa
Brand Name : Bezalip
Dosage Form : TAB
Dosage Strength : 200mg
Packaging : 90X1mg
Approval Date :
Application Number :
Regulatory Info : Originator
Registration Country : South Africa
Regulatory Info : Originator
Registration Country : South Africa
Brand Name : Bezalip Retard
Dosage Form : TAB
Dosage Strength : 400mg
Packaging : 30X1mg
Approval Date :
Application Number :
Regulatory Info : Originator
Registration Country : South Africa
Regulatory Info : Deregistered
Registration Country : Sweden
Brand Name : Bezalip Retard
Dosage Form : Tablet
Dosage Strength : 400mg
Packaging :
Approval Date : 31/05/2002
Application Number : 20020531000045
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 : Bezalip Retard
Dosage Form : Tablet
Dosage Strength : 400mg
Packaging :
Approval Date : 07/10/1999
Application Number : 19991007000088
Regulatory Info : Deregistered
Registration Country : Sweden
Portfolio PDF
Product Web Link
Virtual Booth
Digital Content
Website
Corporate PDF