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
01 77TABLET;ORAL
01 55DISCN
02 22RX
01 4ACCUPRIL
02 3ACCURETIC
03 52QUINAPRIL HYDROCHLORIDE
04 18QUINAPRIL HYDROCHLORIDE AND HYDROCHLOROTHIAZIDE
01 70No
02 7Yes
RLD : No
TE Code :
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 :
RLD : No
TE Code :
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 :
RLD : No
TE Code :
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 :
RLD : Yes
TE Code :
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Dosage Strength : EQ 5MG BASE **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons**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 :
RLD : Yes
TE Code :
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Dosage Strength : EQ 10MG BASE **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons**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 :
RLD : Yes
TE Code :
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Dosage Strength : EQ 20MG BASE **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons**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 :
RLD : Yes
TE Code :
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Dosage Strength : EQ 40MG BASE **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons**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 :
RLD : Yes
TE Code :
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 :
RLD : Yes
TE Code :
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 :
RLD : Yes
TE Code :
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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