Orange Book product · Generic (ANDA)
BENAZEPRIL HYDROCHLORIDE
BENAZEPRIL HYDROCHLORIDE
At a glance
May 22, 2008
Approved
Generic (ANDA)
Application
AB
TE code
None
Listed patents
Key dates
Approval
FDA approval date of this drug product.
May 22, 2008
18 yr 4 mo ago
Today
Pharmaceutical detail
Active ingredient
BENAZEPRIL HYDROCHLORIDE
Strength
10MG
Dosage form
TABLET
Route
ORAL
TE code
AB
Application
ANDA 078212
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
- 1991LOTENSINBrand (NDA)
NDA 019851 · VALIDUS PHARMS
- 2008BENAZEPRIL HYDROCHLORIDEGeneric (ANDA)
ANDA 078848 · ZYDUS LIFESCIENCES
- 2006BENAZEPRIL HYDROCHLORIDEGeneric (ANDA)
ANDA 077128 · COREPHARMA
- 2006BENAZEPRIL HYDROCHLORIDEGeneric (ANDA)
ANDA 076820 · AMNEAL PHARMS
- 2004BENAZEPRIL HYDROCHLORIDEGeneric (ANDA)
ANDA 076333 · ANI PHARMS
- 2004BENAZEPRIL HYDROCHLORIDEGeneric (ANDA)
ANDA 076402 · CHARTWELL RX
- 2004BENAZEPRIL HYDROCHLORIDEGeneric (ANDA)
ANDA 076476 · GENPHARM
- 2004BENAZEPRIL HYDROCHLORIDEGeneric (ANDA)
ANDA 076267 · HERITAGE PHARMA
- 2004BENAZEPRIL HYDROCHLORIDEGeneric (ANDA)
ANDA 076118 · PRINSTON INC
- 2004BENAZEPRIL HYDROCHLORIDEGeneric (ANDA)
ANDA 076430 · RISING
- 2004BENAZEPRIL HYDROCHLORIDEGeneric (ANDA)
ANDA 076344 · SUN PHARM INDS LTD
- 2004BENAZEPRIL HYDROCHLORIDEGeneric (ANDA)
ANDA 076211 · TEVA
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.
