Active Ingredient: DICYCLOMINE HYDROCHLORIDE
Proprietary Name: DICYCLOMINE HYDROCHLORIDE
Dosage Form; Route of Administration: TABLET; ORAL
Strength: 20MG
Reference Listed Drug: No
Reference Standard: Yes
TE Code: AB
Application Number: A085223
Product Number: 001
Approval Date: Jul 30, 1986
Applicant Holder Full Name: WATSON LABORATORIES INC
Marketing Status:
Prescription
Patent and Exclusivity Information