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: A040586
Product Number: 002
Approval Date: Feb 24, 2005
Applicant Holder Full Name: OXFORD PHARMACEUTICALS LLC
Marketing Status:
Prescription
Patent and Exclusivity Information