Active Ingredient: PRIMIDONE
Proprietary Name: PRIMIDONE
Dosage Form; Route of Administration: TABLET; ORAL
Strength: 250MG
Reference Listed Drug: No
Reference Standard: No
TE Code:
Application Number: A040667
Product Number: 002
Approval Date: Jul 27, 2006
Applicant Holder Full Name: HIKMA INTERNATIONAL PHARMACEUTICALS LLC
Marketing Status:
Discontinued
Patent and Exclusivity Information
