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: A216390
Product Number: 001
Approval Date: Dec 23, 2022
Applicant Holder Full Name: STERISCIENCE PTE LTD
Marketing Status:
Prescription
Patent and Exclusivity Information