Orange Book: Approved Drug Products with Therapeutic Equivalence Evaluations

Home | Back to Search Results

Product Details for ANDA 075480

Expand all

ENALAPRIL MALEATE (ENALAPRIL MALEATE)
2.5MG
Marketing Status: Discontinued

Active Ingredient: ENALAPRIL MALEATE
Proprietary Name: ENALAPRIL MALEATE
Dosage Form; Route of Administration: TABLET; ORAL
Strength: 2.5MG
Reference Listed Drug: No
Reference Standard: No
TE Code: 
Application Number: A075480
Product Number: 001
Approval Date: Aug 22, 2000
Applicant Holder Full Name: AUROBINDO PHARMA USA INC
Marketing Status:  Discontinued
Patent and Exclusivity Information

ENALAPRIL MALEATE (ENALAPRIL MALEATE)
5MG
Marketing Status: Discontinued

Active Ingredient: ENALAPRIL MALEATE
Proprietary Name: ENALAPRIL MALEATE
Dosage Form; Route of Administration: TABLET; ORAL
Strength: 5MG
Reference Listed Drug: No
Reference Standard: No
TE Code: 
Application Number: A075480
Product Number: 002
Approval Date: Aug 22, 2000
Applicant Holder Full Name: AUROBINDO PHARMA USA INC
Marketing Status:  Discontinued
Patent and Exclusivity Information

ENALAPRIL MALEATE (ENALAPRIL MALEATE)
10MG
Marketing Status: Discontinued

Active Ingredient: ENALAPRIL MALEATE
Proprietary Name: ENALAPRIL MALEATE
Dosage Form; Route of Administration: TABLET; ORAL
Strength: 10MG
Reference Listed Drug: No
Reference Standard: No
TE Code: 
Application Number: A075480
Product Number: 003
Approval Date: Aug 22, 2000
Applicant Holder Full Name: AUROBINDO PHARMA USA INC
Marketing Status:  Discontinued
Patent and Exclusivity Information

ENALAPRIL MALEATE (ENALAPRIL MALEATE)
20MG
Marketing Status: Discontinued

Active Ingredient: ENALAPRIL MALEATE
Proprietary Name: ENALAPRIL MALEATE
Dosage Form; Route of Administration: TABLET; ORAL
Strength: 20MG
Reference Listed Drug: No
Reference Standard: No
TE Code: 
Application Number: A075480
Product Number: 004
Approval Date: Aug 22, 2000
Applicant Holder Full Name: AUROBINDO PHARMA USA INC
Marketing Status:  Discontinued
Patent and Exclusivity Information