Orange Book product · Generic (ANDA)
QUINAPRIL HYDROCHLORIDE AND HYDROCHLOROTHIAZIDE
HYDROCHLOROTHIAZIDE; QUINAPRIL HYDROCHLORIDE
At a glance
Mar 31, 2004
Approved
Generic (ANDA)
Application
AB
TE code
None
Listed patents
Key dates
Approval
FDA approval date of this drug product.
Mar 31, 2004
22 yr 7 mo ago
Today
Pharmaceutical detail
Active ingredient
HYDROCHLOROTHIAZIDE; QUINAPRIL HYDROCHLORIDE
Strength
12.5MG;EQ 10MG BASE
Dosage form
TABLET
Route
ORAL
TE code
AB
Application
ANDA 076374
Product number
001
Marketing status
RX
Reference listed drug (RLD)
No
Reference standard (RS)
No
Active-ingredient family
View full familyGeneric (ANDA) of HYDROCHLOROTHIAZIDE; QUINAPRIL HYDROCHLORIDE
- 1999ACCURETICBrand (NDA)
NDA 020125 · PFIZER PHARMS
- 2013QUINAPRIL HYDROCHLORIDE AND HYDROCHLOROTHIAZIDEGeneric (ANDA)
ANDA 091524 · APOTEX
- 2011QUINAPRIL HYDROCHLORIDE AND HYDROCHLOROTHIAZIDEGeneric (ANDA)
ANDA 201356 · INVAGEN PHARMS
- 2009QUINAPRIL HYDROCHLORIDE AND HYDROCHLOROTHIAZIDEGeneric (ANDA)
ANDA 078211 · SUN PHARM INDS LTD
- 2007QUINAPRIL HYDROCHLORIDE AND HYDROCHLOROTHIAZIDEGeneric (ANDA)
ANDA 078450 · AUROBINDO PHARMA
- 2005QUINAPRIL HYDROCHLORIDE AND HYDROCHLOROTHIAZIDEGeneric (ANDA)
ANDA 077093 · PHARMOBEDIENT
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.
