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01 1Allergan Aesthetics

02 1Aspen Pharmacare Holdings

03 2Aurobindo Pharma Limited

04 2Aurovitas Spain, Sau

05 1Bial

06 1HENNIG ARZNEIMITTEL

07 1Ivax Scandinavia Ab

08 1JAMP PHARMA

09 4Karo Pharma

10 1Medreich

11 1National Pharma

12 3ORIFARM GROUP AS

13 1Paranova Pharmaceuticals Ab

14 1Pharma Dynamics

15 1Pharma Regulatory Services Limited

16 1Pharmascience Inc.

17 1Sandoz B2B

18 3Teva Pharmaceutical Industries

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PharmaCompass

01

BEZAFIBRATE

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

Abbvie CB

02

Bezafibrate

Brand Name : Bezachole Sr

Dosage Form : TAB

Dosage Strength : 400mg

Packaging : 30X1mg

Approval Date :

Application Number :

Regulatory Info : Generic

Registration Country : South Africa

Aspen API Comapny Banner

03

CPhI India
Not Confirmed
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CPhI India
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

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04

CPhI India
Not Confirmed
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CPhI India
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

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05

CPhI India
Not Confirmed
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CPhI India
Not Confirmed

Bezafibrate

Brand Name : Difaterol Retard

Dosage Form : Extended-Release Tablet

Dosage Strength : 400MG

Packaging :

Approval Date : 1987-04-01

Application Number : 57184

Regulatory Info : Cancelled

Registration Country : Spain

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06

CPhI India
Not Confirmed
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CPhI India
Not Confirmed

BEZAFIBRATE

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

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07

CPhI India
Not Confirmed
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CPhI India
Not Confirmed

Bezafibrate

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

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08

CPhI India
Not Confirmed
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CPhI India
Not Confirmed

Bezafibrate

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

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09

CPhI India
Not Confirmed
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CPhI India
Not Confirmed

Bezafibrate

Brand Name :

Dosage Form : Sustained Release Tablet

Dosage Strength : 400MG

Packaging :

Approval Date :

Application Number :

Regulatory Info :

Registration Country : India

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10

CPhI India
Not Confirmed
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CPhI India
Not Confirmed

Bezafibrate

Brand Name :

Dosage Form : Tablet

Dosage Strength : 40MG

Packaging :

Approval Date :

Application Number :

Regulatory Info :

Registration Country : India

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11

CPhI India
Not Confirmed
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CPhI India
Not Confirmed

Bezafibrate

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

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12

CPhI India
Not Confirmed
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CPhI India
Not Confirmed

Bezafibrate

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

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13

CPhI India
Not Confirmed
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CPhI India
Not Confirmed

Bezafibrate

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

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14

CPhI India
Not Confirmed
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CPhI India
Not Confirmed

Bezafibrate

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

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15

CPhI India
Not Confirmed
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CPhI India
Not Confirmed

Bezafibrate

Brand Name : PMS-BEZAFIBRATE

Dosage Form : TABLET

Dosage Strength : 200MG

Packaging : 30/100

Approval Date :

Application Number :

Regulatory Info : Prescription

Registration Country : Canada

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16

CPhI India
Not Confirmed
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CPhI India
Not Confirmed

Bezafibrate

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

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17

Ivax Scandinavia Ab

Country
CPhI India
Not Confirmed
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Ivax Scandinavia Ab

Country
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CPhI India
Not Confirmed

Bezafibrate

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

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18

Paranova Pharmaceuticals Ab

Country
CPhI India
Not Confirmed
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Paranova Pharmaceuticals Ab

Country
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CPhI India
Not Confirmed

Bezafibrate

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

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19

Aurovitas Spain, Sau

Country
CPhI India
Not Confirmed
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Aurovitas Spain, Sau

Country
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CPhI India
Not Confirmed

Bezafibrate

Brand Name : Eulitop Retard

Dosage Form : Extended-Release Tablet

Dosage Strength : 400MG

Packaging :

Approval Date : 1986-10-01

Application Number : 57150

Regulatory Info : Authorized

Registration Country : Spain

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20

Aurovitas Spain, Sau

Country
CPhI India
Not Confirmed
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Aurovitas Spain, Sau

Country
arrow
CPhI India
Not Confirmed

Bezafibrate

Brand Name : Eulitop

Dosage Form : Film Coated Tablet

Dosage Strength : 200MG

Packaging :

Approval Date : 1981-12-01

Application Number : 55728

Regulatory Info : Authorized

Registration Country : Spain

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