Active Ingredient: PHENYTOIN SODIUM
Proprietary Name: PHENYTOIN SODIUM
Dosage Form; Route of Administration: INJECTABLE; INJECTION
Strength: 50MG/ML
Reference Listed Drug: No
Reference Standard: No
TE Code: AP
Application Number: A040573
Product Number: 001
Approval Date: Sep 13, 2006
Applicant Holder Full Name: ACELLA PHARMACEUTICALS LLC
Marketing Status:
Prescription
Patent and Exclusivity Information