Orange Book product · Generic (ANDA)
QUINAPRIL HYDROCHLORIDE AND HYDROCHLOROTHIAZIDE
HYDROCHLOROTHIAZIDE; QUINAPRIL HYDROCHLORIDE
At a glance
Aug 24, 2007
Approved
Generic (ANDA)
Application
AB
TE code
None
Listed patents
Key dates
Approval
FDA approval date of this drug product.
Aug 24, 2007
19 yr 1 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 078450
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
- 2005QUINAPRIL HYDROCHLORIDE AND HYDROCHLOROTHIAZIDEGeneric (ANDA)
ANDA 077093 · PHARMOBEDIENT
- 2004QUINAPRIL HYDROCHLORIDE AND HYDROCHLOROTHIAZIDEGeneric (ANDA)
ANDA 076374 · CHARTWELL RX
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.
