Active Ingredient: DICYCLOMINE HYDROCHLORIDE
Proprietary Name: DICYCLOMINE HYDROCHLORIDE
Dosage Form; Route of Administration: INJECTABLE; INJECTION
Strength: 10MG/ML
Reference Listed Drug: No
Reference Standard: No
TE Code:
Application Number: A207084
Product Number: 001
Approval Date: May 4, 2018
Applicant Holder Full Name: RENEW PHARMACEUTICALS LTD
Marketing Status:
Discontinued
Patent and Exclusivity Information