Active Ingredient: HYDROXYCHLOROQUINE SULFATE
Proprietary Name: HYDROXYCHLOROQUINE SULFATE
Dosage Form; Route of Administration: TABLET; ORAL
Strength: 200MG
Reference Listed Drug: No
Reference Standard: No
TE Code: AB
Application Number: A212902
Product Number: 001
Approval Date: May 14, 2020
Applicant Holder Full Name: SENORES PHARMACEUTICALS INC
Marketing Status:
Prescription
Patent and Exclusivity Information
