Active Ingredient: FOSPHENYTOIN SODIUM
Proprietary Name: FOSPHENYTOIN SODIUM
Dosage Form; Route of Administration: INJECTABLE; INJECTION
Strength: EQ 50MG PHENYTOIN NA/ML
Reference Listed Drug: No
Reference Standard: No
TE Code: AP
Application Number: A078765
Product Number: 001
Approval Date: Dec 2, 2009
Applicant Holder Full Name: HIKMA FARMACEUTICA (PORTUGAL) SA
Marketing Status:
Prescription
Patent and Exclusivity Information