Active Ingredient: NITAZOXANIDE
Proprietary Name: NITAZOXANIDE
Dosage Form; Route of Administration: TABLET; ORAL
Strength: 500MG
Reference Listed Drug: No
Reference Standard: No
TE Code: AB
Application Number: A218701
Product Number: 001
Approval Date: Apr 15, 2025
Applicant Holder Full Name: ANNORA PHARMA PRIVATE LTD
Marketing Status:
Prescription
Patent and Exclusivity Information
