Active Ingredient: DEXMEDETOMIDINE HYDROCHLORIDE
Proprietary Name: DEXMEDETOMIDINE HYDROCHLORIDE
Dosage Form; Route of Administration: INJECTABLE; INJECTION
Strength: EQ 200MCG BASE/2ML (EQ 100MCG BASE/ML)
Reference Listed Drug: No
Reference Standard: No
TE Code: AP
Application Number: A202126
Product Number: 001
Approval Date: Aug 20, 2015
Applicant Holder Full Name: GLAND PHARMA LTD
Marketing Status:
Prescription
Patent and Exclusivity Information