Active Ingredient: TRIPROLIDINE HYDROCHLORIDE
Proprietary Name: ACTIDIL
Dosage Form; Route of Administration: TABLET; ORAL
Strength: 2.5MG
Reference Listed Drug: No
Reference Standard: No
TE Code:
Application Number: N011110
Product Number: 002
Approval Date: Jul 1, 1983
Applicant Holder Full Name: GLAXOSMITHKLINE
Marketing Status:
Discontinued
Patent and Exclusivity Information
