Please Wait
Applying Filters...
Menu
Xls
Filters Filter
Cross PopUp
FILTER :

filter clear-filterReset all filters

01 2APOTEX INC

02 5CHARTWELL RX

03 3GLENMARK PHARMS

04 2GLENMARK PHARMS LTD

05 3HERITAGE

06 5TEVA

07 5UCB INC

filter clear-filterReset all filters

filter clear-filterReset all filters

filter clear-filterReset all filters

filter clear-filterReset all filters

PharmaCompass

01

Pharmtech & Ingredients
Not Confirmed
arrow
arrow
Pharmtech & Ingredients
Not Confirmed

MOEXIPRIL HYDROCHLORIDE

Brand Name : MOEXIPRIL HYDROCHLORIDE

Dosage Form : TABLET;ORAL

Dosage Strength : 7.5MG

Approval Date : 2003-05-08

Application Number : 76204

RX/OTC/DISCN : RX

RLD : No

TE Code : AB

blank

02

Pharmtech & Ingredients
Not Confirmed
arrow
arrow
Pharmtech & Ingredients
Not Confirmed

MOEXIPRIL HYDROCHLORIDE

Brand Name : MOEXIPRIL HYDROCHLORIDE

Dosage Form : TABLET;ORAL

Dosage Strength : 15MG

Approval Date : 2003-05-08

Application Number : 76204

RX/OTC/DISCN : RX

RLD : No

TE Code : AB

blank

03

Pharmtech & Ingredients
Not Confirmed
arrow
arrow
Pharmtech & Ingredients
Not Confirmed

HYDROCHLOROTHIAZIDE; MOEXIPRIL HYDROCHLORIDE

Brand Name : MOEXIPRIL HYDROCHLORIDE AND HYDROCHLOROTHIAZIDE

Dosage Form : TABLET;ORAL

Dosage Strength : 12.5MG;7.5MG

Approval Date : 2007-03-07

Application Number : 76980

RX/OTC/DISCN : RX

RLD : No

TE Code : AB

blank

04

Pharmtech & Ingredients
Not Confirmed
arrow
arrow
Pharmtech & Ingredients
Not Confirmed

HYDROCHLOROTHIAZIDE; MOEXIPRIL HYDROCHLORIDE

Brand Name : MOEXIPRIL HYDROCHLORIDE AND HYDROCHLOROTHIAZIDE

Dosage Form : TABLET;ORAL

Dosage Strength : 25MG;15MG

Approval Date : 2007-03-07

Application Number : 76980

RX/OTC/DISCN : RX

RLD : No

TE Code : AB

blank

05

Pharmtech & Ingredients
Not Confirmed
arrow
arrow
Pharmtech & Ingredients
Not Confirmed

HYDROCHLOROTHIAZIDE; MOEXIPRIL HYDROCHLORIDE

Brand Name : MOEXIPRIL HYDROCHLORIDE AND HYDROCHLOROTHIAZIDE

Dosage Form : TABLET;ORAL

Dosage Strength : 12.5MG;15MG

Approval Date : 2007-03-07

Application Number : 76980

RX/OTC/DISCN : RX

RLD : No

TE Code : AB

blank

06

Pharmtech & Ingredients
Not Confirmed
arrow
arrow
Pharmtech & Ingredients
Not Confirmed

MOEXIPRIL HYDROCHLORIDE

Brand Name : UNIVASC

Dosage Form : TABLET;ORAL

Dosage Strength : 7.5MG **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons**

Approval Date : 1995-04-19

Application Number : 20312

RX/OTC/DISCN : DISCN

RLD : No

TE Code :

blank

07

Pharmtech & Ingredients
Not Confirmed
arrow
arrow
Pharmtech & Ingredients
Not Confirmed

MOEXIPRIL HYDROCHLORIDE

Brand Name : UNIVASC

Dosage Form : TABLET;ORAL

Dosage Strength : 15MG **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons**

Approval Date : 1995-04-19

Application Number : 20312

RX/OTC/DISCN : DISCN

RLD : No

TE Code :

blank

08

Pharmtech & Ingredients
Not Confirmed
arrow
arrow
Pharmtech & Ingredients
Not Confirmed

HYDROCHLOROTHIAZIDE; MOEXIPRIL HYDROCHLORIDE

Brand Name : UNIRETIC

Dosage Form : TABLET;ORAL

Dosage Strength : 12.5MG;7.5MG **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons**

Approval Date : 1997-06-27

Application Number : 20729

RX/OTC/DISCN : DISCN

RLD : No

TE Code :

blank

09

Pharmtech & Ingredients
Not Confirmed
arrow
arrow
Pharmtech & Ingredients
Not Confirmed

HYDROCHLOROTHIAZIDE; MOEXIPRIL HYDROCHLORIDE

Brand Name : UNIRETIC

Dosage Form : TABLET;ORAL

Dosage Strength : 25MG;15MG **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons**

Approval Date : 1997-06-27

Application Number : 20729

RX/OTC/DISCN : DISCN

RLD : No

TE Code :

blank

10

Pharmtech & Ingredients
Not Confirmed
arrow
arrow
Pharmtech & Ingredients
Not Confirmed

HYDROCHLOROTHIAZIDE; MOEXIPRIL HYDROCHLORIDE

Brand Name : UNIRETIC

Dosage Form : TABLET;ORAL

Dosage Strength : 12.5MG;15MG **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons**

Approval Date : 2002-02-14

Application Number : 20729

RX/OTC/DISCN : DISCN

RLD : No

TE Code :

blank