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: AP
Application Number: A204473
Product Number: 001
Approval Date: Aug 31, 2017
Applicant Holder Full Name: ZYDUS PHARMACEUTICALS USA INC
Marketing Status:
Prescription
Patent and Exclusivity Information
