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01 1Allergan Aesthetics
02 1Aspen Pharmacare Holdings
03 2Aurobindo Pharma Limited
04 1Ivax Scandinavia Ab
05 1JAMP PHARMA
06 2Karo Pharma
07 1Medreich
08 1National Pharma
09 3ORIFARM GROUP AS
10 1Paranova Pharmaceuticals Ab
11 1Pharma Dynamics
12 1Pharmascience Inc.
13 1Sandoz B2B
14 3Teva Pharmaceutical Industries
15 2Blank
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01 2Bezafibrate 400Mg 30 Joined' Oral Use Rp
02 2Film Coated Tablet
03 3Modified Release Tablet
04 1SRT
05 1Sustained Release Tablet
06 4TAB
07 1TABLET
08 2TABLET (EXTENDED-RELEASE)
09 6Tablet
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01 1Allowed
02 2Approved
03 5Deregistered
04 3Generic
05 2Originator
06 1Prescription
07 8Blank
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01 1BEZALIP SR
02 1Bezachole Sr
03 1Bezafibrate
04 4Bezalip
05 6Bezalip Retard
06 1Cedur retard
07 1Difaterol Retard 400Mg 30 Tablets
08 1Dyna Bezafibrate Sr 400
09 1Eulitop Retard 30 Tablets
10 1JAMP-BEZAFIBRATE SR
11 1PMS-BEZAFIBRATE
12 1Sandoz Bezafibrate 400
13 2Blank
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01 3Canada
02 2India
03 2Italy
04 5South Africa
05 2Spain
06 7Sweden
07 1Switzerland
Regulatory Info :
Registration Country : Canada
Brand Name : BEZALIP SR
Dosage Form : TABLET (EXTENDED-RELEASE)
Dosage Strength : 400MG
Packaging : 30
Approval Date :
Application Number : 2083523
Regulatory Info :
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 :
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 :
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 : 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 :
Registration Country : Spain
Brand Name : Difaterol Retard 400Mg 30 Tablets
Dosage Form : Modified Release Tablet
Dosage Strength : 400 Mg/modified release tablet
Packaging :
Approval Date :
Application Number :
Regulatory Info :
Registration Country : Spain
Portfolio PDF
Product Web Link
Virtual Booth
Digital Content
Website
Corporate PDF
Regulatory Info :
Registration Country : Spain
Brand Name : Eulitop Retard 30 Tablets
Dosage Form : Modified Release Tablet
Dosage Strength : 400 Mg/modified release tablet
Packaging :
Approval Date :
Application Number :
Regulatory Info :
Registration Country : Spain
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 : 31/05/2002
Application Number : 20020531000045
Regulatory Info : Deregistered
Registration Country : Sweden
Portfolio PDF
Product Web Link
Virtual Booth
Digital Content
Website
Corporate PDF