Orange Book product · Generic (ANDA)
QUINAPRIL HYDROCHLORIDE
QUINAPRIL HYDROCHLORIDE
At a glance
Jun 20, 2006
Approved
Generic (ANDA)
Application
AB
TE code
None
Listed patents
Key dates
Approval
FDA approval date of this drug product.
Jun 20, 2006
20 yr 3 mo ago
Today
Pharmaceutical detail
Active ingredient
QUINAPRIL HYDROCHLORIDE
Strength
EQ 5MG BASE
Dosage form
TABLET
Route
ORAL
TE code
AB
Application
ANDA 077690
Product number
001
Marketing status
RX
Reference listed drug (RLD)
No
Reference standard (RS)
No
Active-ingredient family
View full familyGeneric (ANDA) of QUINAPRIL HYDROCHLORIDE
- 1991ACCUPRILBrand (NDA)
NDA 019885 · PFIZER PHARMS
- 2016QUINAPRIL HYDROCHLORIDEGeneric (ANDA)
ANDA 205823 · PRINSTON INC
- 2013QUINAPRIL HYDROCHLORIDEGeneric (ANDA)
ANDA 202725 · AUROBINDO PHARMA LTD
- 2009QUINAPRIL HYDROCHLORIDEGeneric (ANDA)
ANDA 090800 · SUN PHARM INDS LTD
- 2007QUINAPRIL HYDROCHLORIDEGeneric (ANDA)
ANDA 075504 · ANI PHARMS
- 2007QUINAPRIL HYDROCHLORIDEGeneric (ANDA)
ANDA 078457 · INVAGEN PHARMS
- 2006QUINAPRIL HYDROCHLORIDEGeneric (ANDA)
ANDA 076240 · APOTEX INC
- 2005QUINAPRIL HYDROCHLORIDEGeneric (ANDA)
ANDA 076803 · CHARTWELL RX
- 2005QUINAPRIL HYDROCHLORIDEGeneric (ANDA)
ANDA 076036 · MYLAN
- 2005QUINAPRIL HYDROCHLORIDEGeneric (ANDA)
ANDA 076049 · ACTAVIS LABS FL INC
- 2004QUINAPRIL HYDROCHLORIDEGeneric (ANDA)
ANDA 076694 · PHARMOBEDIENT
- 2004QUINAPRIL HYDROCHLORIDEGeneric (ANDA)
ANDA 076459 · ACTAVIS ELIZABETH
Listed patents
No patents are listed against this product in the Orange Book. Listed patents reflect those the NDA holder submits under 21 U.S.C. 355 and are not exhaustive.

