Active Ingredient: PRIMIDONE
Proprietary Name: PRIMIDONE
Dosage Form; Route of Administration: TABLET; ORAL
Strength: 250MG
Reference Listed Drug: No
Reference Standard: No
TE Code: AB
Application Number: A214896
Product Number: 002
Approval Date: Jun 28, 2022
Applicant Holder Full Name: RUBICON RESEARCH PRIVATE LTD
Marketing Status:
Prescription
Patent and Exclusivity Information