Active Ingredient: MYCOPHENOLATE MOFETIL HYDROCHLORIDE
Proprietary Name: MYCOPHENOLATE MOFETIL HYDROCHLORIDE
Dosage Form; Route of Administration: INJECTABLE; INJECTION
Strength: 500MG/VIAL
Reference Listed Drug: No
Reference Standard: No
TE Code:
Application Number: A211374
Product Number: 001
Approval Date: Mar 5, 2021
Applicant Holder Full Name: AMNEAL EU LTD
Marketing Status:
Discontinued
Patent and Exclusivity Information