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: A084903
Product Number: 001
Approval Date: Approved Prior to Jan 1, 1982
Applicant Holder Full Name: LANNETT CO INC
Marketing Status:
Prescription
Patent and Exclusivity Information