Orange Book: Approved Drug Products with Therapeutic Equivalence Evaluations

Home | Back to Search Results

Product Details for ANDA 090441

Expand all

IMIPRAMINE HYDROCHLORIDE (IMIPRAMINE HYDROCHLORIDE)
10MG
Marketing Status: Discontinued

Active Ingredient: IMIPRAMINE HYDROCHLORIDE
Proprietary Name: IMIPRAMINE HYDROCHLORIDE
Dosage Form; Route of Administration: TABLET; ORAL
Strength: 10MG
Reference Listed Drug: No
Reference Standard: No
TE Code: 
Application Number: A090441
Product Number: 002
Approval Date: Mar 11, 2010
Applicant Holder Full Name: CHARTWELL LIFE MOLECULES LLC
Marketing Status:  Discontinued
Patent and Exclusivity Information

IMIPRAMINE HYDROCHLORIDE (IMIPRAMINE HYDROCHLORIDE)
25MG
Marketing Status: Discontinued

Active Ingredient: IMIPRAMINE HYDROCHLORIDE
Proprietary Name: IMIPRAMINE HYDROCHLORIDE
Dosage Form; Route of Administration: TABLET; ORAL
Strength: 25MG
Reference Listed Drug: No
Reference Standard: No
TE Code: 
Application Number: A090441
Product Number: 003
Approval Date: Mar 11, 2010
Applicant Holder Full Name: CHARTWELL LIFE MOLECULES LLC
Marketing Status:  Discontinued
Patent and Exclusivity Information

IMIPRAMINE HYDROCHLORIDE (IMIPRAMINE HYDROCHLORIDE)
50MG
Marketing Status: Discontinued

Active Ingredient: IMIPRAMINE HYDROCHLORIDE
Proprietary Name: IMIPRAMINE HYDROCHLORIDE
Dosage Form; Route of Administration: TABLET; ORAL
Strength: 50MG
Reference Listed Drug: No
Reference Standard: No
TE Code: 
Application Number: A090441
Product Number: 001
Approval Date: Mar 11, 2010
Applicant Holder Full Name: CHARTWELL LIFE MOLECULES LLC
Marketing Status:  Discontinued
Patent and Exclusivity Information