Orange Book: Approved Drug Products with Therapeutic Equivalence Evaluations

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Product Details for NDA 019558

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PRINIVIL (LISINOPRIL)
5MG
Marketing Status: Prescription
Active Ingredient: LISINOPRIL
Proprietary Name: PRINIVIL
Dosage Form; Route of Administration: TABLET; ORAL
Strength: 5MG
Reference Listed Drug: No
Reference Standard: No
TE Code: AB
Application Number: N019558
Product Number: 001
Approval Date: Dec 29, 1987
Applicant Holder Full Name: MERCK RESEARCH LABORATORIES DIV MERCK CO INC
Marketing Status:  Prescription
Patent and Exclusivity Information
PRINIVIL (LISINOPRIL)
40MG
Marketing Status: Prescription
Active Ingredient: LISINOPRIL
Proprietary Name: PRINIVIL
Dosage Form; Route of Administration: TABLET; ORAL
Strength: 40MG
Reference Listed Drug: No
Reference Standard: No
TE Code: AB
Application Number: N019558
Product Number: 004
Approval Date: Oct 25, 1988
Applicant Holder Full Name: MERCK RESEARCH LABORATORIES DIV MERCK CO INC
Marketing Status:  Prescription
Patent and Exclusivity Information
PRINIVIL (LISINOPRIL)
2.5MG
Marketing Status: Discontinued
Active Ingredient: LISINOPRIL
Proprietary Name: PRINIVIL
Dosage Form; Route of Administration: TABLET; ORAL
Strength: 2.5MG
Reference Listed Drug: No
Reference Standard: No
TE Code: 
Application Number: N019558
Product Number: 006
Approval Date: Jan 28, 1994
Applicant Holder Full Name: MERCK RESEARCH LABORATORIES DIV MERCK CO INC
Marketing Status:  Discontinued
Patent and Exclusivity Information
PRINIVIL (LISINOPRIL)
10MG
Marketing Status: Discontinued
Active Ingredient: LISINOPRIL
Proprietary Name: PRINIVIL
Dosage Form; Route of Administration: TABLET; ORAL
Strength: 10MG
Reference Listed Drug: No
Reference Standard: No
TE Code: 
Application Number: N019558
Product Number: 002
Approval Date: Dec 29, 1987
Applicant Holder Full Name: MERCK RESEARCH LABORATORIES DIV MERCK CO INC
Marketing Status:  Discontinued
Patent and Exclusivity Information
PRINIVIL (LISINOPRIL)
20MG
Marketing Status: Discontinued
Active Ingredient: LISINOPRIL
Proprietary Name: PRINIVIL
Dosage Form; Route of Administration: TABLET; ORAL
Strength: 20MG
Reference Listed Drug: No
Reference Standard: No
TE Code: 
Application Number: N019558
Product Number: 003
Approval Date: Dec 29, 1987
Applicant Holder Full Name: MERCK RESEARCH LABORATORIES DIV MERCK CO INC
Marketing Status:  Discontinued
Patent and Exclusivity Information

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