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 076342
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 076348 · ANI PHARMS
- 2004BENAZEPRIL HYDROCHLORIDE AND HYDROCHLOROTHIAZIDEGeneric (ANDA)
ANDA 076688 · AUROBINDO PHARMA USA
- 2004BENAZEPRIL HYDROCHLORIDE AND HYDROCHLOROTHIAZIDEGeneric (ANDA)
ANDA 076612 · MYLAN PHARMS INC
- 2004BENAZEPRIL HYDROCHLORIDE AND HYDROCHLOROTHIAZIDEGeneric (ANDA)
ANDA 076631 · SANDOZ
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.
