Active Ingredient: DICYCLOMINE HYDROCHLORIDE
Proprietary Name: DICYCLOMINE HYDROCHLORIDE
Dosage Form; Route of Administration: TABLET; ORAL
Strength: 20MG
Reference Listed Drug: No
Reference Standard: No
TE Code: AB
Application Number: A040161
Product Number: 001
Approval Date: Oct 1, 1996
Applicant Holder Full Name: HIKMA PHARMACEUTICALS
Marketing Status:
Prescription
Patent and Exclusivity Information
