Active Ingredient: MYCOPHENOLIC SODIUM
Proprietary Name: MYFORTIC
Dosage Form; Route of Administration: TABLET, DELAYED RELEASE; ORAL
Strength: EQ 360MG BASE
Reference Listed Drug: Yes
Reference Standard: Yes
TE Code: AB
Application Number: N050791
Product Number: 002
Approval Date: Feb 27, 2004
Applicant Holder Full Name: NOVARTIS PHARMACEUTICALS CORP
Marketing Status:
Prescription
Patent and Exclusivity Information