Active Ingredient: ACYCLOVIR
Proprietary Name: ACYCLOVIR
Dosage Form; Route of Administration: SUSPENSION; ORAL
Strength: 200MG/5ML
Reference Listed Drug: No
Reference Standard: No
TE Code: AB
Application Number: A215724
Product Number: 001
Approval Date: Aug 18, 2022
Applicant Holder Full Name: RUBICON RESEARCH PRIVATE LTD
Marketing Status:
Prescription
Patent and Exclusivity Information
