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: AP
Application Number: A210257
Product Number: 001
Approval Date: Jan 25, 2019
Applicant Holder Full Name: FRESENIUS KABI USA LLC
Marketing Status:
Prescription
Patent and Exclusivity Information