Active Ingredient: LOPERAMIDE HYDROCHLORIDE; SIMETHICONE
Proprietary Name: LOPERAMIDE HYDROCHLORIDE AND SIMETHICONE
Dosage Form; Route of Administration: TABLET; ORAL
Strength: 2MG;125MG
Reference Listed Drug: No
Reference Standard: No
TE Code:
Application Number: A077500
Product Number: 001
Approval Date: Sep 6, 2006
Applicant Holder Full Name: SUN PHARMACEUTICAL INDUSTRIES LTD
Marketing Status:
Discontinued
Patent and Exclusivity Information
