Active Ingredient: DESIPRAMINE HYDROCHLORIDE
Proprietary Name: DESIPRAMINE HYDROCHLORIDE
Dosage Form; Route of Administration: TABLET; ORAL
Strength: 75MG
Reference Listed Drug: No
Reference Standard: No
TE Code: AB
Application Number: A071602
Product Number: 001
Approval Date: Oct 5, 1987
Applicant Holder Full Name: ACTAVIS TOTOWA LLC
Marketing Status:
Prescription
Patent and Exclusivity Information