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:
Application Number: A076886
Product Number: 001
Approval Date: Aug 6, 2007
Applicant Holder Full Name: DR REDDYS LABORATORIES LTD
Marketing Status:
Discontinued
Patent and Exclusivity Information