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 217900

LEQSELVI (DEURUXOLITINIB PHOSPHATE)
EQ 8MG BASE
Marketing Status: Prescription
Active Ingredient: DEURUXOLITINIB PHOSPHATE
Proprietary Name: LEQSELVI
Dosage Form; Route of Administration: TABLET; ORAL
Strength: EQ 8MG BASE
Reference Listed Drug: Yes
Reference Standard: Yes
TE Code: 
Application Number: N217900
Product Number: 001
Approval Date: Jul 25, 2024
Applicant Holder Full Name: SUN PHARMACEUTICAL INDUSTRIES INC
Marketing Status:  Prescription
Patent and Exclusivity Information
Back to Top