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: A040657
Product Number: 001
Approval Date: Sep 21, 2007
Applicant Holder Full Name: ZYDUS PHARMACEUTICALS USA INC
Marketing Status:
Prescription
Patent and Exclusivity Information
