Product Details for NDA 019885
ACCUPRIL (QUINAPRIL HYDROCHLORIDE)
EQ 5MG BASE **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons**
Marketing Status: Discontinued
EQ 10MG BASE **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons**
Marketing Status: Discontinued
EQ 20MG BASE **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons**
Marketing Status: Discontinued
EQ 40MG BASE **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons**
Marketing Status: Discontinued
EQ 5MG BASE **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons**
Marketing Status: Discontinued
Active Ingredient: QUINAPRIL HYDROCHLORIDE
Proprietary Name: ACCUPRIL
Dosage Form; Route of Administration: TABLET; ORAL
Strength: EQ 5MG BASE **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons**
Reference Listed Drug: Yes
Reference Standard: No
TE Code:
Application Number: N019885
Product Number: 001
Approval Date: Nov 19, 1991
Applicant Holder Full Name: PFIZER PHARMACEUTICALS LTD
Marketing Status: Discontinued
Patent and Exclusivity Information
ACCUPRIL (QUINAPRIL HYDROCHLORIDE)
Proprietary Name: ACCUPRIL
Dosage Form; Route of Administration: TABLET; ORAL
Strength: EQ 5MG BASE **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons**
Reference Listed Drug: Yes
Reference Standard: No
TE Code:
Application Number: N019885
Product Number: 001
Approval Date: Nov 19, 1991
Applicant Holder Full Name: PFIZER PHARMACEUTICALS LTD
Marketing Status: Discontinued
Patent and Exclusivity Information
EQ 10MG BASE **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons**
Marketing Status: Discontinued
Active Ingredient: QUINAPRIL HYDROCHLORIDE
Proprietary Name: ACCUPRIL
Dosage Form; Route of Administration: TABLET; ORAL
Strength: EQ 10MG BASE **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons**
Reference Listed Drug: Yes
Reference Standard: No
TE Code:
Application Number: N019885
Product Number: 002
Approval Date: Nov 19, 1991
Applicant Holder Full Name: PFIZER PHARMACEUTICALS LTD
Marketing Status: Discontinued
Patent and Exclusivity Information
ACCUPRIL (QUINAPRIL HYDROCHLORIDE)
Proprietary Name: ACCUPRIL
Dosage Form; Route of Administration: TABLET; ORAL
Strength: EQ 10MG BASE **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons**
Reference Listed Drug: Yes
Reference Standard: No
TE Code:
Application Number: N019885
Product Number: 002
Approval Date: Nov 19, 1991
Applicant Holder Full Name: PFIZER PHARMACEUTICALS LTD
Marketing Status: Discontinued
Patent and Exclusivity Information
EQ 20MG BASE **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons**
Marketing Status: Discontinued
Active Ingredient: QUINAPRIL HYDROCHLORIDE
Proprietary Name: ACCUPRIL
Dosage Form; Route of Administration: TABLET; ORAL
Strength: EQ 20MG BASE **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons**
Reference Listed Drug: Yes
Reference Standard: No
TE Code:
Application Number: N019885
Product Number: 003
Approval Date: Nov 19, 1991
Applicant Holder Full Name: PFIZER PHARMACEUTICALS LTD
Marketing Status: Discontinued
Patent and Exclusivity Information
ACCUPRIL (QUINAPRIL HYDROCHLORIDE)
Proprietary Name: ACCUPRIL
Dosage Form; Route of Administration: TABLET; ORAL
Strength: EQ 20MG BASE **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons**
Reference Listed Drug: Yes
Reference Standard: No
TE Code:
Application Number: N019885
Product Number: 003
Approval Date: Nov 19, 1991
Applicant Holder Full Name: PFIZER PHARMACEUTICALS LTD
Marketing Status: Discontinued
Patent and Exclusivity Information
EQ 40MG BASE **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons**
Marketing Status: Discontinued
Active Ingredient: QUINAPRIL HYDROCHLORIDE
Proprietary Name: ACCUPRIL
Dosage Form; Route of Administration: TABLET; ORAL
Strength: EQ 40MG BASE **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons**
Reference Listed Drug: Yes
Reference Standard: No
TE Code:
Application Number: N019885
Product Number: 004
Approval Date: Nov 19, 1991
Applicant Holder Full Name: PFIZER PHARMACEUTICALS LTD
Marketing Status: Discontinued
Patent and Exclusivity Information
Proprietary Name: ACCUPRIL
Dosage Form; Route of Administration: TABLET; ORAL
Strength: EQ 40MG BASE **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons**
Reference Listed Drug: Yes
Reference Standard: No
TE Code:
Application Number: N019885
Product Number: 004
Approval Date: Nov 19, 1991
Applicant Holder Full Name: PFIZER PHARMACEUTICALS LTD
Marketing Status: Discontinued
Patent and Exclusivity Information