Active Ingredient: ATROPINE SULFATE; DIPHENOXYLATE HYDROCHLORIDE
Proprietary Name: LOMOTIL
Dosage Form; Route of Administration: TABLET; ORAL
Strength: 0.025MG;2.5MG
Reference Listed Drug: Yes
Reference Standard: Yes
TE Code: AA
Application Number: N012462
Product Number: 001
Approval Date: Approved Prior to Jan 1, 1982
Applicant Holder Full Name: PFIZER INC
Marketing Status:
Prescription
Patent and Exclusivity Information