Active Ingredient: ANILERIDINE HYDROCHLORIDE
Proprietary Name: LERITINE
Dosage Form; Route of Administration: TABLET; ORAL
Strength: EQ 25MG BASE
Reference Listed Drug: No
Reference Standard: No
TE Code:
Application Number: N010585
Product Number: 002
Approval Date: Approved Prior to Jan 1, 1982
Applicant Holder Full Name: MERCK AND CO INC
Marketing Status:
Discontinued
Patent and Exclusivity Information
