Orange Book product · Generic (ANDA)
BENAZEPRIL HYDROCHLORIDE AND HYDROCHLOROTHIAZIDE
BENAZEPRIL HYDROCHLORIDE; HYDROCHLOROTHIAZIDE
At a glance
Feb 11, 2004
Approved
Generic (ANDA)
Application
AB
TE code
None
Listed patents
Key dates
Approval
FDA approval date of this drug product.
Feb 11, 2004
22 yr 8 mo ago
Today
Pharmaceutical detail
Active ingredient
BENAZEPRIL HYDROCHLORIDE; HYDROCHLOROTHIAZIDE
Strength
5MG;6.25MG
Dosage form
TABLET
Route
ORAL
TE code
AB
Application
ANDA 076631
Product number
001
Marketing status
RX
Reference listed drug (RLD)
No
Reference standard (RS)
No
Active-ingredient family
View full familyGeneric (ANDA) of BENAZEPRIL HYDROCHLORIDE; HYDROCHLOROTHIAZIDE
- 1992LOTENSIN HCTBrand (NDA)
NDA 020033 · VALIDUS PHARMS
- 2014BENAZEPRIL HYDROCHLORIDE AND HYDROCHLOROTHIAZIDEGeneric (ANDA)
ANDA 078794 · APOTEX
- 2005BENAZEPRIL HYDROCHLORIDE AND HYDROCHLOROTHIAZIDEGeneric (ANDA)
ANDA 077483 · SUN PHARM INDS LTD
- 2004BENAZEPRIL HYDROCHLORIDE AND HYDROCHLOROTHIAZIDEGeneric (ANDA)
ANDA 076342 · ANI PHARMS
- 2004BENAZEPRIL HYDROCHLORIDE AND HYDROCHLOROTHIAZIDEGeneric (ANDA)
ANDA 076348 · ANI PHARMS
- 2004BENAZEPRIL HYDROCHLORIDE AND HYDROCHLOROTHIAZIDEGeneric (ANDA)
ANDA 076688 · AUROBINDO PHARMA USA
- 2004BENAZEPRIL HYDROCHLORIDE AND HYDROCHLOROTHIAZIDEGeneric (ANDA)
ANDA 076612 · MYLAN PHARMS INC
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.
