Product Details for ANDA 076459
QUINAPRIL HYDROCHLORIDE (QUINAPRIL HYDROCHLORIDE)
EQ 5MG BASE
Marketing Status: Discontinued
EQ 10MG BASE
Marketing Status: Discontinued
EQ 20MG BASE
Marketing Status: Discontinued
EQ 40MG BASE
Marketing Status: Discontinued
EQ 5MG BASE
Marketing Status: Discontinued
Active Ingredient: QUINAPRIL HYDROCHLORIDE
Proprietary Name: QUINAPRIL HYDROCHLORIDE
Dosage Form; Route of Administration: TABLET; ORAL
Strength: EQ 5MG BASE
Reference Listed Drug: No
Reference Standard: No
TE Code:
Application Number: A076459
Product Number: 001
Approval Date: Dec 22, 2004
Applicant Holder Full Name: ACTAVIS ELIZABETH LLC
Marketing Status: Discontinued
Patent and Exclusivity Information
QUINAPRIL HYDROCHLORIDE (QUINAPRIL HYDROCHLORIDE)
Proprietary Name: QUINAPRIL HYDROCHLORIDE
Dosage Form; Route of Administration: TABLET; ORAL
Strength: EQ 5MG BASE
Reference Listed Drug: No
Reference Standard: No
TE Code:
Application Number: A076459
Product Number: 001
Approval Date: Dec 22, 2004
Applicant Holder Full Name: ACTAVIS ELIZABETH LLC
Marketing Status: Discontinued
Patent and Exclusivity Information
EQ 10MG BASE
Marketing Status: Discontinued
Active Ingredient: QUINAPRIL HYDROCHLORIDE
Proprietary Name: QUINAPRIL HYDROCHLORIDE
Dosage Form; Route of Administration: TABLET; ORAL
Strength: EQ 10MG BASE
Reference Listed Drug: No
Reference Standard: No
TE Code:
Application Number: A076459
Product Number: 002
Approval Date: Dec 22, 2004
Applicant Holder Full Name: ACTAVIS ELIZABETH LLC
Marketing Status: Discontinued
Patent and Exclusivity Information
QUINAPRIL HYDROCHLORIDE (QUINAPRIL HYDROCHLORIDE)
Proprietary Name: QUINAPRIL HYDROCHLORIDE
Dosage Form; Route of Administration: TABLET; ORAL
Strength: EQ 10MG BASE
Reference Listed Drug: No
Reference Standard: No
TE Code:
Application Number: A076459
Product Number: 002
Approval Date: Dec 22, 2004
Applicant Holder Full Name: ACTAVIS ELIZABETH LLC
Marketing Status: Discontinued
Patent and Exclusivity Information
EQ 20MG BASE
Marketing Status: Discontinued
Active Ingredient: QUINAPRIL HYDROCHLORIDE
Proprietary Name: QUINAPRIL HYDROCHLORIDE
Dosage Form; Route of Administration: TABLET; ORAL
Strength: EQ 20MG BASE
Reference Listed Drug: No
Reference Standard: No
TE Code:
Application Number: A076459
Product Number: 003
Approval Date: Dec 22, 2004
Applicant Holder Full Name: ACTAVIS ELIZABETH LLC
Marketing Status: Discontinued
Patent and Exclusivity Information
QUINAPRIL HYDROCHLORIDE (QUINAPRIL HYDROCHLORIDE)
Proprietary Name: QUINAPRIL HYDROCHLORIDE
Dosage Form; Route of Administration: TABLET; ORAL
Strength: EQ 20MG BASE
Reference Listed Drug: No
Reference Standard: No
TE Code:
Application Number: A076459
Product Number: 003
Approval Date: Dec 22, 2004
Applicant Holder Full Name: ACTAVIS ELIZABETH LLC
Marketing Status: Discontinued
Patent and Exclusivity Information
EQ 40MG BASE
Marketing Status: Discontinued
Active Ingredient: QUINAPRIL HYDROCHLORIDE
Proprietary Name: QUINAPRIL HYDROCHLORIDE
Dosage Form; Route of Administration: TABLET; ORAL
Strength: EQ 40MG BASE
Reference Listed Drug: No
Reference Standard: No
TE Code:
Application Number: A076459
Product Number: 004
Approval Date: Dec 22, 2004
Applicant Holder Full Name: ACTAVIS ELIZABETH LLC
Marketing Status: Discontinued
Patent and Exclusivity Information
Proprietary Name: QUINAPRIL HYDROCHLORIDE
Dosage Form; Route of Administration: TABLET; ORAL
Strength: EQ 40MG BASE
Reference Listed Drug: No
Reference Standard: No
TE Code:
Application Number: A076459
Product Number: 004
Approval Date: Dec 22, 2004
Applicant Holder Full Name: ACTAVIS ELIZABETH LLC
Marketing Status: Discontinued
Patent and Exclusivity Information