Product Details for ANDA 078211
QUINAPRIL HYDROCHLORIDE AND HYDROCHLOROTHIAZIDE (HYDROCHLOROTHIAZIDE; QUINAPRIL HYDROCHLORIDE)
12.5MG;EQ 10MG BASE
Marketing Status: Discontinued
12.5MG;EQ 20MG BASE
Marketing Status: Discontinued
25MG;EQ 20MG BASE
Marketing Status: Discontinued
12.5MG;EQ 10MG BASE
Marketing Status: Discontinued
Active Ingredient: HYDROCHLOROTHIAZIDE; QUINAPRIL HYDROCHLORIDE
Proprietary Name: QUINAPRIL HYDROCHLORIDE AND HYDROCHLOROTHIAZIDE
Dosage Form; Route of Administration: TABLET; ORAL
Strength: 12.5MG;EQ 10MG BASE
Reference Listed Drug: No
Reference Standard: No
TE Code:
Application Number: A078211
Product Number: 001
Approval Date: Mar 4, 2009
Applicant Holder Full Name: SUN PHARMACEUTICAL INDUSTRIES LTD
Marketing Status: Discontinued
Patent and Exclusivity Information
QUINAPRIL HYDROCHLORIDE AND HYDROCHLOROTHIAZIDE (HYDROCHLOROTHIAZIDE; QUINAPRIL HYDROCHLORIDE)
Proprietary Name: QUINAPRIL HYDROCHLORIDE AND HYDROCHLOROTHIAZIDE
Dosage Form; Route of Administration: TABLET; ORAL
Strength: 12.5MG;EQ 10MG BASE
Reference Listed Drug: No
Reference Standard: No
TE Code:
Application Number: A078211
Product Number: 001
Approval Date: Mar 4, 2009
Applicant Holder Full Name: SUN PHARMACEUTICAL INDUSTRIES LTD
Marketing Status: Discontinued
Patent and Exclusivity Information
12.5MG;EQ 20MG BASE
Marketing Status: Discontinued
Active Ingredient: HYDROCHLOROTHIAZIDE; QUINAPRIL HYDROCHLORIDE
Proprietary Name: QUINAPRIL HYDROCHLORIDE AND HYDROCHLOROTHIAZIDE
Dosage Form; Route of Administration: TABLET; ORAL
Strength: 12.5MG;EQ 20MG BASE
Reference Listed Drug: No
Reference Standard: No
TE Code:
Application Number: A078211
Product Number: 002
Approval Date: Mar 4, 2009
Applicant Holder Full Name: SUN PHARMACEUTICAL INDUSTRIES LTD
Marketing Status: Discontinued
Patent and Exclusivity Information
QUINAPRIL HYDROCHLORIDE AND HYDROCHLOROTHIAZIDE (HYDROCHLOROTHIAZIDE; QUINAPRIL HYDROCHLORIDE)
Proprietary Name: QUINAPRIL HYDROCHLORIDE AND HYDROCHLOROTHIAZIDE
Dosage Form; Route of Administration: TABLET; ORAL
Strength: 12.5MG;EQ 20MG BASE
Reference Listed Drug: No
Reference Standard: No
TE Code:
Application Number: A078211
Product Number: 002
Approval Date: Mar 4, 2009
Applicant Holder Full Name: SUN PHARMACEUTICAL INDUSTRIES LTD
Marketing Status: Discontinued
Patent and Exclusivity Information
25MG;EQ 20MG BASE
Marketing Status: Discontinued
Active Ingredient: HYDROCHLOROTHIAZIDE; QUINAPRIL HYDROCHLORIDE
Proprietary Name: QUINAPRIL HYDROCHLORIDE AND HYDROCHLOROTHIAZIDE
Dosage Form; Route of Administration: TABLET; ORAL
Strength: 25MG;EQ 20MG BASE
Reference Listed Drug: No
Reference Standard: No
TE Code:
Application Number: A078211
Product Number: 003
Approval Date: Mar 4, 2009
Applicant Holder Full Name: SUN PHARMACEUTICAL INDUSTRIES LTD
Marketing Status: Discontinued
Patent and Exclusivity Information
Proprietary Name: QUINAPRIL HYDROCHLORIDE AND HYDROCHLOROTHIAZIDE
Dosage Form; Route of Administration: TABLET; ORAL
Strength: 25MG;EQ 20MG BASE
Reference Listed Drug: No
Reference Standard: No
TE Code:
Application Number: A078211
Product Number: 003
Approval Date: Mar 4, 2009
Applicant Holder Full Name: SUN PHARMACEUTICAL INDUSTRIES LTD
Marketing Status: Discontinued
Patent and Exclusivity Information