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Product Details for ANDA 076688

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BENAZEPRIL HYDROCHLORIDE AND HYDROCHLOROTHIAZIDE (BENAZEPRIL HYDROCHLORIDE; HYDROCHLOROTHIAZIDE)
5MG;6.25MG
Marketing Status: Discontinued

Active Ingredient: BENAZEPRIL HYDROCHLORIDE; HYDROCHLOROTHIAZIDE
Proprietary Name: BENAZEPRIL HYDROCHLORIDE AND HYDROCHLOROTHIAZIDE
Dosage Form; Route of Administration: TABLET; ORAL
Strength: 5MG;6.25MG
Reference Listed Drug: No
Reference Standard: No
TE Code: 
Application Number: A076688
Product Number: 001
Approval Date: Feb 11, 2004
Applicant Holder Full Name: AUROBINDO PHARMA USA INC
Marketing Status:  Discontinued
Patent and Exclusivity Information

BENAZEPRIL HYDROCHLORIDE AND HYDROCHLOROTHIAZIDE (BENAZEPRIL HYDROCHLORIDE; HYDROCHLOROTHIAZIDE)
10MG;12.5MG
Marketing Status: Discontinued

Active Ingredient: BENAZEPRIL HYDROCHLORIDE; HYDROCHLOROTHIAZIDE
Proprietary Name: BENAZEPRIL HYDROCHLORIDE AND HYDROCHLOROTHIAZIDE
Dosage Form; Route of Administration: TABLET; ORAL
Strength: 10MG;12.5MG
Reference Listed Drug: No
Reference Standard: No
TE Code: 
Application Number: A076688
Product Number: 002
Approval Date: Feb 11, 2004
Applicant Holder Full Name: AUROBINDO PHARMA USA INC
Marketing Status:  Discontinued
Patent and Exclusivity Information

BENAZEPRIL HYDROCHLORIDE AND HYDROCHLOROTHIAZIDE (BENAZEPRIL HYDROCHLORIDE; HYDROCHLOROTHIAZIDE)
20MG;12.5MG
Marketing Status: Discontinued

Active Ingredient: BENAZEPRIL HYDROCHLORIDE; HYDROCHLOROTHIAZIDE
Proprietary Name: BENAZEPRIL HYDROCHLORIDE AND HYDROCHLOROTHIAZIDE
Dosage Form; Route of Administration: TABLET; ORAL
Strength: 20MG;12.5MG
Reference Listed Drug: No
Reference Standard: No
TE Code: 
Application Number: A076688
Product Number: 003
Approval Date: Feb 11, 2004
Applicant Holder Full Name: AUROBINDO PHARMA USA INC
Marketing Status:  Discontinued
Patent and Exclusivity Information

BENAZEPRIL HYDROCHLORIDE AND HYDROCHLOROTHIAZIDE (BENAZEPRIL HYDROCHLORIDE; HYDROCHLOROTHIAZIDE)
20MG;25MG
Marketing Status: Discontinued

Active Ingredient: BENAZEPRIL HYDROCHLORIDE; HYDROCHLOROTHIAZIDE
Proprietary Name: BENAZEPRIL HYDROCHLORIDE AND HYDROCHLOROTHIAZIDE
Dosage Form; Route of Administration: TABLET; ORAL
Strength: 20MG;25MG
Reference Listed Drug: No
Reference Standard: No
TE Code: 
Application Number: A076688
Product Number: 004
Approval Date: Feb 11, 2004
Applicant Holder Full Name: AUROBINDO PHARMA USA INC
Marketing Status:  Discontinued
Patent and Exclusivity Information