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: AB
Application Number: A081050
Product Number: 001
Approval Date: Jun 5, 1990
Applicant Holder Full Name: SUN PHARMACEUTICAL INDUSTRIES INC
Marketing Status:
Prescription
Patent and Exclusivity Information