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: A087631
Product Number: 001
Approval Date: Jan 4, 1982
Applicant Holder Full Name: VANGARD LABORATORIES INC DIV MIDWAY MEDICAL CO
Marketing Status:
Discontinued
Patent and Exclusivity Information