Active Ingredient: DESIPRAMINE HYDROCHLORIDE
Proprietary Name: DESIPRAMINE HYDROCHLORIDE
Dosage Form; Route of Administration: TABLET; ORAL
Strength: 100MG
Reference Listed Drug: No
Reference Standard: No
TE Code:
Application Number: A071867
Product Number: 001
Approval Date: Sep 9, 1987
Applicant Holder Full Name: USL PHARMA INC
Marketing Status:
Discontinued
Patent and Exclusivity Information