Please Wait
Applying Filters...
Menu
$ API Ref.Price (USD/KG) : 101Xls
Filters Filter
Cross PopUp
FILTER :

filter clear-filterReset all filters

01 2AUROBINDO PHARMA ITALIA Srl

02 2Actavis Group PTC ehf

03 2Actavis Group Ptc Ehf.

04 2Aurovitas Spain, Sau

05 1Bial Laboratories Sa

06 1Hennig Arzneimittel GmbH & Co KG

07 1Ivax Scandinavia Ab

08 3Orifarm Ab

09 1Paranova Pharmaceuticals Ab

10 1Pharma Regulatory Services Limited

11 1Teva Pharma Ag

filter clear-filterReset all filters

filter clear-filterReset all filters

filter clear-filterReset all filters

filter clear-filterReset all filters

PharmaCompass

01

International Sweetener Colloquium
Not Confirmed
arrow
arrow
International Sweetener Colloquium
Not Confirmed

Bezafibrate

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

blank

02

International Sweetener Colloquium
Not Confirmed
arrow
arrow
International Sweetener Colloquium
Not Confirmed

Bezafibrate

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

blank

03

International Sweetener Colloquium
Not Confirmed
arrow
arrow
International Sweetener Colloquium
Not Confirmed

Bezafibrate

Brand Name : Difaterol Retard

Dosage Form : Extended-Release Tablet

Dosage Strength : 400MG

Packaging :

Approval Date : 01-04-1987

Application Number : 57184

Regulatory Info : Cancelled

Registration Country : Spain

blank

04

International Sweetener Colloquium
Not Confirmed
arrow
arrow
International Sweetener Colloquium
Not Confirmed

Bezafibrate

Brand Name : Befibrat

Dosage Form : Film Coated Tablet

Dosage Strength : 400MG

Packaging :

Approval Date : 2006-11-01

Application Number :

Regulatory Info : Withdrawn

Registration Country : Malta

blank

05

International Sweetener Colloquium
Not Confirmed
arrow
arrow
International Sweetener Colloquium
Not Confirmed

Bezafibrate

Brand Name : Bezalip

Dosage Form : Film Coated Tablet

Dosage Strength : 200MG

Packaging :

Approval Date : 2009-01-22

Application Number :

Regulatory Info : Withdrawn

Registration Country : Malta

blank

06

International Sweetener Colloquium
Not Confirmed
arrow
arrow
International Sweetener Colloquium
Not Confirmed

Bezafibrate

Brand Name : Bezalip Mono

Dosage Form : Modified Release Tablet

Dosage Strength : 400MG

Packaging :

Approval Date : 2009-01-22

Application Number :

Regulatory Info : Withdrawn

Registration Country : Malta

blank

07

International Sweetener Colloquium
Not Confirmed
arrow
arrow
International Sweetener Colloquium
Not Confirmed

Bezafibrate

Brand Name : Bezalip

Dosage Form : Film Coated Tablet

Dosage Strength : 200mg

Packaging :

Approval Date : 28-09-1990

Application Number : 1.99E+13

Regulatory Info : Approved

Registration Country : Sweden

blank

08

International Sweetener Colloquium
Not Confirmed
arrow
arrow
International Sweetener Colloquium
Not Confirmed

Bezafibrate

Brand Name : Bezalip Retard

Dosage Form : Tablet

Dosage Strength : 400mg

Packaging :

Approval Date : 29-06-1994

Application Number : 1.99E+13

Regulatory Info : Approved

Registration Country : Sweden

blank

09

Aurovitas Spain, Sau

Country
International Sweetener Colloquium
Not Confirmed
arrow

Aurovitas Spain, Sau

Country
arrow
International Sweetener Colloquium
Not Confirmed

Bezafibrate

Brand Name : Eulitop Retard

Dosage Form : Extended-Release Tablet

Dosage Strength : 400MG

Packaging :

Approval Date : 01-10-1986

Application Number : 57150

Regulatory Info : Authorized

Registration Country : Spain

blank

10

Aurovitas Spain, Sau

Country
International Sweetener Colloquium
Not Confirmed
arrow

Aurovitas Spain, Sau

Country
arrow
International Sweetener Colloquium
Not Confirmed

Bezafibrate

Brand Name : Eulitop

Dosage Form : Film Coated Tablet

Dosage Strength : 200MG

Packaging :

Approval Date : 01-12-1981

Application Number : 55728

Regulatory Info : Authorized

Registration Country : Spain

blank