Active Ingredient: FEBUXOSTAT
Proprietary Name: FEBUXOSTAT
Dosage Form; Route of Administration: TABLET; ORAL
Strength: 40MG
Reference Listed Drug: No
Reference Standard: No
TE Code: AB
Application Number: A206266
Product Number: 001
Approval Date: Mar 28, 2022
Applicant Holder Full Name: PRINSTON PHARMACEUTICAL INC
Marketing Status:
Prescription
Patent and Exclusivity Information