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01 4ACTAVIS ELIZABETH

02 4ACTAVIS LABS FL INC

03 4ANI PHARMS

04 3APOTEX

05 4APOTEX INC

06 3AUROBINDO PHARMA

07 4AUROBINDO PHARMA LTD

08 7CHARTWELL RX

09 7INVAGEN PHARMS

10 4LUPIN

11 4MYLAN

12 7NORVIUM BIOSCIENCE

13 7PFIZER PHARMS

14 4PRINSTON INC

15 11SUN PHARM INDS LTD

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PharmaCompass

01

Pharma, Lab & Chemical Expo
Not Confirmed
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Pharma, Lab & Chemical Expo
Not Confirmed

QUINAPRIL HYDROCHLORIDE

Brand Name : QUINAPRIL HYDROCHLORIDE

Dosage Form : TABLET;ORAL

Dosage Strength : EQ 5MG BASE

Approval Date : 2007-08-24

Application Number : 75504

RX/OTC/DISCN : DISCN

RLD : No

TE Code :

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02

Pharma, Lab & Chemical Expo
Not Confirmed
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Pharma, Lab & Chemical Expo
Not Confirmed

QUINAPRIL HYDROCHLORIDE

Brand Name : QUINAPRIL HYDROCHLORIDE

Dosage Form : TABLET;ORAL

Dosage Strength : EQ 10MG BASE

Approval Date : 2007-08-24

Application Number : 75504

RX/OTC/DISCN : DISCN

RLD : No

TE Code :

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03

Pharma, Lab & Chemical Expo
Not Confirmed
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Pharma, Lab & Chemical Expo
Not Confirmed

QUINAPRIL HYDROCHLORIDE

Brand Name : QUINAPRIL HYDROCHLORIDE

Dosage Form : TABLET;ORAL

Dosage Strength : EQ 20MG BASE

Approval Date : 2007-08-24

Application Number : 75504

RX/OTC/DISCN : DISCN

RLD : No

TE Code :

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04

Pharma, Lab & Chemical Expo
Not Confirmed
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Pharma, Lab & Chemical Expo
Not Confirmed

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Dosage Strength : EQ 5MG BASE **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons**

Approval Date : 1991-11-19

Application Number : 19885

RX/OTC/DISCN : DISCN

RLD : Yes

TE Code :

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05

Pharma, Lab & Chemical Expo
Not Confirmed
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Pharma, Lab & Chemical Expo
Not Confirmed

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Dosage Strength : EQ 10MG BASE **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons**

Approval Date : 1991-11-19

Application Number : 19885

RX/OTC/DISCN : DISCN

RLD : Yes

TE Code :

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06

Pharma, Lab & Chemical Expo
Not Confirmed
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Pharma, Lab & Chemical Expo
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**

Approval Date : 1991-11-19

Application Number : 19885

RX/OTC/DISCN : DISCN

RLD : Yes

TE Code :

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07

Pharma, Lab & Chemical Expo
Not Confirmed
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Pharma, Lab & Chemical Expo
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**

Approval Date : 1991-11-19

Application Number : 19885

RX/OTC/DISCN : DISCN

RLD : Yes

TE Code :

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08

Pharma, Lab & Chemical Expo
Not Confirmed
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Pharma, Lab & Chemical Expo
Not Confirmed

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**

Approval Date : 1999-12-28

Application Number : 20125

RX/OTC/DISCN : DISCN

RLD : Yes

TE Code :

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09

Pharma, Lab & Chemical Expo
Not Confirmed
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Pharma, Lab & Chemical Expo
Not Confirmed

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**

Approval Date : 1999-12-28

Application Number : 20125

RX/OTC/DISCN : DISCN

RLD : Yes

TE Code :

blank

10

Pharma, Lab & Chemical Expo
Not Confirmed
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Pharma, Lab & Chemical Expo
Not Confirmed

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**

Approval Date : 1999-12-28

Application Number : 20125

RX/OTC/DISCN : DISCN

RLD : Yes

TE Code :

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