U.S. flag An official website of the United States government
  1. Home
  2. Drug Databases
  3. Orange Book Home

Orange Book: Approved Drug Products with Therapeutic Equivalence Evaluations

Home | Back to Search Results

Product Details for NDA 218033

OJEMDA (TOVORAFENIB)
25MG/ML
Marketing Status: Prescription
Active Ingredient: TOVORAFENIB
Proprietary Name: OJEMDA
Dosage Form; Route of Administration: FOR SUSPENSION; ORAL
Strength: 25MG/ML
Reference Listed Drug: Yes
Reference Standard: Yes
TE Code: 
Application Number: N218033
Product Number: 001
Approval Date: Apr 23, 2024
Applicant Holder Full Name: DAY ONE BIOPHARMACEUTICALS INC
Marketing Status:  Prescription
Patent and Exclusivity Information
Back to Top