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01 2Aspen Pharmacare Holdings

02 2Orion Corporation

03 4ANI Pharmaceuticals Inc

04 8Actavis Inc

05 2Adcock Ingram

06 9Apotex Inc

07 1Arrow Pharmaceuticals

08 4Assia Chemical Industries Ltd

09 12Aurobindo Pharma Limited

10 2Aurogen South Africa (Pty) Ltd

11 1Aurovitas Spain, Sau

12 1BENEDETTI & CO.SpA

13 7Chartwell Pharmaceuticals llc

14 3Cinfa

15 2Daiichi Sankyo

16 2EG SpA

17 2EG Spa

18 4Heumann

19 8Hexal AG

20 7InvaGen Pharmaceuticals Inc

21 3Karo Pharma

22 2LABORATORIOS NORMON SA

23 4Lacer

24 4Lupin Ltd

25 3MALESCI SpA IST.FARMACOBIOL.

26 2Malesci Istituto Farmacobiologico

27 7Medis ehff

28 3Menarini

29 2Novagen Pharma

30 4ORIFARM GROUP AS

31 7PHARMOBEDIENT

32 25Pfizer Inc

33 4Pharma Dynamics

34 4Pharmascience Inc.

35 4Prinston

36 12Ratiopharm GmbH

37 4Recordati

38 12STADA Arzneimittel

39 3Sandoz B2B

40 11Sun Pharmaceutical Industries Limited

41 3Tamarang

42 4Teva Pharmaceutical Industries

43 10Viatris

44 4Winthrop Arzneimittel Gmbh

45 4Winthrop Medicaments

46 5Zentiva

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PharmaCompass

01

Quinapril

Brand Name : Quinaspen

Dosage Form : TAB

Dosage Strength : 20mg

Packaging : 30X1mg

Approval Date :

Application Number :

Regulatory Info : Generic

Registration Country : South Africa

Aspen API Comapny Banner

02

Hydrochlorthiazide; Quinapril Hydrochloride

Brand Name : Quinapril/Hydrochlorothiazid Orion

Dosage Form : Film Coated Tablet

Dosage Strength : 10mg;12.5mg

Packaging :

Approval Date : 30/04/2004

Application Number : 20040430000380

Regulatory Info : Deregistered

Registration Country : Sweden

Fermion Orion Company Banner

03

Quinapril

Brand Name : Quinaspen 10 mg

Dosage Form : TAB

Dosage Strength : 10mg

Packaging : 30X1mg

Approval Date :

Application Number :

Regulatory Info : Generic

Registration Country : South Africa

Aspen API Comapny Banner

04

Hydrochlorthiazide; Quinapril Hydrochloride

Brand Name : Quinapril/Hydrochlorothiazid Orion

Dosage Form : Film Coated Tablet

Dosage Strength : 20mg;12.5mg

Packaging :

Approval Date : 30/04/2004

Application Number : 20040430000397

Regulatory Info : Deregistered

Registration Country : Sweden

Fermion Orion Company Banner

05

PREP
Not Confirmed
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QUINAPRIL HYDROCHLORIDE

Brand Name : QUINAPRIL HYDROCHLORIDE

Dosage Form : TABLET;ORAL

Dosage Strength : EQ 5MG BASE

Packaging :

Approval Date : 2005-01-14

Application Number : 76049

Regulatory Info : DISCN

Registration Country : USA

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06

PREP
Not Confirmed
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QUINAPRIL HYDROCHLORIDE

Brand Name : QUINAPRIL HYDROCHLORIDE

Dosage Form : TABLET;ORAL

Dosage Strength : EQ 5MG BASE

Packaging :

Approval Date : 2007-08-24

Application Number : 75504

Regulatory Info : DISCN

Registration Country : USA

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07

PREP
Not Confirmed
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PREP
Not Confirmed

QUINAPRIL HYDROCHLORIDE

Brand Name : QUINAPRIL HYDROCHLORIDE

Dosage Form : TABLET;ORAL

Dosage Strength : EQ 10MG BASE

Packaging :

Approval Date : 2007-08-24

Application Number : 75504

Regulatory Info : DISCN

Registration Country : USA

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08

PREP
Not Confirmed
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QUINAPRIL HYDROCHLORIDE

Brand Name : QUINAPRIL HYDROCHLORIDE

Dosage Form : TABLET;ORAL

Dosage Strength : EQ 20MG BASE

Packaging :

Approval Date : 2007-08-24

Application Number : 75504

Regulatory Info : DISCN

Registration Country : USA

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09

PREP
Not Confirmed
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QUINAPRIL HYDROCHLORIDE

Brand Name : QUINAPRIL HYDROCHLORIDE

Dosage Form : TABLET;ORAL

Dosage Strength : EQ 40MG BASE

Packaging :

Approval Date : 2007-08-24

Application Number : 75504

Regulatory Info : DISCN

Registration Country : USA

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10

PREP
Not Confirmed
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QUINAPRIL HYDROCHLORIDE

Brand Name : ACCUPRIL

Dosage Form : TABLET;ORAL

Dosage Strength : EQ 5MG BASE **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons**

Packaging :

Approval Date : 1991-11-19

Application Number : 19885

Regulatory Info : DISCN

Registration Country : USA

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11

PREP
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QUINAPRIL HYDROCHLORIDE

Brand Name : ACCUPRIL

Dosage Form : TABLET;ORAL

Dosage Strength : EQ 10MG BASE **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons**

Packaging :

Approval Date : 1991-11-19

Application Number : 19885

Regulatory Info : DISCN

Registration Country : USA

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12

PREP
Not Confirmed
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PREP
Not Confirmed

QUINAPRIL HYDROCHLORIDE

Brand Name : ACCUPRIL

Dosage Form : TABLET;ORAL

Dosage Strength : EQ 20MG BASE **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons**

Packaging :

Approval Date : 1991-11-19

Application Number : 19885

Regulatory Info : DISCN

Registration Country : USA

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13

PREP
Not Confirmed
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PREP
Not Confirmed

QUINAPRIL HYDROCHLORIDE

Brand Name : ACCUPRIL

Dosage Form : TABLET;ORAL

Dosage Strength : EQ 40MG BASE **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons**

Packaging :

Approval Date : 1991-11-19

Application Number : 19885

Regulatory Info : DISCN

Registration Country : USA

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14

PREP
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HYDROCHLOROTHIAZIDE; QUINAPRIL HYDROCHLORIDE

Brand Name : ACCURETIC

Dosage Form : TABLET;ORAL

Dosage Strength : 12.5MG;EQ 10MG BASE **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons**

Packaging :

Approval Date : 1999-12-28

Application Number : 20125

Regulatory Info : DISCN

Registration Country : USA

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15

PREP
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HYDROCHLOROTHIAZIDE; QUINAPRIL HYDROCHLORIDE

Brand Name : ACCURETIC

Dosage Form : TABLET;ORAL

Dosage Strength : 12.5MG;EQ 20MG BASE **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons**

Packaging :

Approval Date : 1999-12-28

Application Number : 20125

Regulatory Info : DISCN

Registration Country : USA

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16

PREP
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HYDROCHLOROTHIAZIDE; QUINAPRIL HYDROCHLORIDE

Brand Name : ACCURETIC

Dosage Form : TABLET;ORAL

Dosage Strength : 25MG;EQ 20MG BASE **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons**

Packaging :

Approval Date : 1999-12-28

Application Number : 20125

Regulatory Info : DISCN

Registration Country : USA

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17

PREP
Not Confirmed
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QUINAPRIL HYDROCHLORIDE

Brand Name : QUINAPRIL HYDROCHLORIDE

Dosage Form : TABLET;ORAL

Dosage Strength : EQ 5MG BASE

Packaging :

Approval Date : 2005-01-28

Application Number : 76036

Regulatory Info : DISCN

Registration Country : USA

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18

PREP
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QUINAPRIL HYDROCHLORIDE

Brand Name : QUINAPRIL HYDROCHLORIDE

Dosage Form : TABLET;ORAL

Dosage Strength : EQ 10MG BASE

Packaging :

Approval Date : 2005-01-28

Application Number : 76036

Regulatory Info : DISCN

Registration Country : USA

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19

PREP
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QUINAPRIL HYDROCHLORIDE

Brand Name : QUINAPRIL HYDROCHLORIDE

Dosage Form : TABLET;ORAL

Dosage Strength : EQ 20MG BASE

Packaging :

Approval Date : 2005-01-28

Application Number : 76036

Regulatory Info : DISCN

Registration Country : USA

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20

PREP
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QUINAPRIL HYDROCHLORIDE

Brand Name : QUINAPRIL HYDROCHLORIDE

Dosage Form : TABLET;ORAL

Dosage Strength : EQ 40MG BASE

Packaging :

Approval Date : 2005-01-28

Application Number : 76036

Regulatory Info : DISCN

Registration Country : USA

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