Active Ingredient: ATROPINE SULFATE; DIPHENOXYLATE HYDROCHLORIDE
Proprietary Name: DIPHENOXYLATE HYDROCHLORIDE AND ATROPINE SULFATE
Dosage Form; Route of Administration: TABLET; ORAL
Strength: 0.025MG;2.5MG
Reference Listed Drug: No
Reference Standard: No
TE Code: AA
Application Number: A085372
Product Number: 001
Approval Date: Approved Prior to Jan 1, 1982
Applicant Holder Full Name: LANNETT CO INC
Marketing Status:
Prescription
Patent and Exclusivity Information