ONESOURCE FDA Friday, December 23, 2022 0.00 Neutral

FDA Approves MYCOPHENOLATE MOFETIL — ONESOURCE SPECIALTY PHARMA LIMITED

ONESOURCE SPECIALTY PHARMA LIMITED announced the approval of intravenous mycophenolate mofetil under ANDA 216390, which could strengthen the biologic immunosuppressant market by expanding access to cost-effective alternatives. This launch diversifies Onesource's product portfolio and capitalizes on strong demand in kidney transplant and autoimmune patient populations.

View original filing at SEC.gov →
AI-generated summary for informational purposes only. Always verify against the original filing. Not investment advice. BriefTape is not a registered investment adviser.

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