Active Ingredient: LOPERAMIDE HYDROCHLORIDE
Proprietary Name: IMODIUM A-D
Dosage Form; Route of Administration: TABLET; ORAL
Strength: 2MG
Reference Listed Drug: Yes
Reference Standard: Yes
TE Code:
Application Number: N019860
Product Number: 001
Approval Date: Nov 22, 1989
Applicant Holder Full Name: JOHNSON AND JOHNSON CONSUMER INC MCNEIL CONSUMER HEALTHCARE DIV
Marketing Status:
Over-the-counter
Patent and Exclusivity Information