Active Ingredient: MAPROTILINE HYDROCHLORIDE
Proprietary Name: MAPROTILINE HYDROCHLORIDE
Dosage Form; Route of Administration: TABLET; ORAL
Strength: 75MG
Reference Listed Drug: No
Reference Standard: No
TE Code:
Application Number: A071945
Product Number: 001
Approval Date: Dec 30, 1987
Applicant Holder Full Name: WATSON LABORATORIES INC
Marketing Status:
Discontinued
Patent and Exclusivity Information