Active Ingredient: LOPERAMIDE HYDROCHLORIDE
Proprietary Name: LOPERAMIDE HYDROCHLORIDE
Dosage Form; Route of Administration: SOLUTION; ORAL
Strength: 1MG/5ML
Reference Listed Drug: No
Reference Standard: No
TE Code:
Application Number: A074991
Product Number: 001
Approval Date: Dec 29, 1997
Applicant Holder Full Name: DURAMED PHARMACEUTICALS INC SUB BARR LABORATORIES INC
Marketing Status:
Discontinued
Patent and Exclusivity Information