01 2APOTEX INC
02 5CHARTWELL RX
03 3GLENMARK PHARMS
04 2GLENMARK PHARMS LTD
05 3HERITAGE
06 5TEVA
07 5UCB INC
01 25TABLET;ORAL
01 11DISCN
02 14RX
01 8MOEXIPRIL HYDROCHLORIDE
02 12MOEXIPRIL HYDROCHLORIDE AND HYDROCHLOROTHIAZIDE
03 3UNIRETIC
04 2UNIVASC
01 25No
RLD : No
TE Code : AB
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
RLD : No
TE Code : AB
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
RLD : No
TE Code : AB
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
RLD : No
TE Code : AB
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
RLD : No
TE Code : AB
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
RLD : No
TE Code :
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Dosage Strength : 7.5MG **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons**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 :
RLD : No
TE Code :
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Dosage Strength : 15MG **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons**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 :
RLD : No
TE Code :
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Dosage Strength : 12.5MG;7.5MG **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons**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 :
RLD : No
TE Code :
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 :
RLD : No
TE Code :
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 :
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