Active Ingredient: ATROPINE SULFATE; DIPHENOXYLATE HYDROCHLORIDE
Proprietary Name: LOMOTIL
Dosage Form; Route of Administration: SOLUTION; ORAL
Strength: 0.025MG/5ML;2.5MG/5ML
Reference Listed Drug: No
Reference Standard: No
TE Code:
Application Number: N012699
Product Number: 001
Approval Date: Approved Prior to Jan 1, 1982
Applicant Holder Full Name: GD SEARLE LLC
Marketing Status:
Discontinued
Patent and Exclusivity Information
