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:
Application Number: A089900
Product Number: 001
Approval Date: Mar 30, 1990
Applicant Holder Full Name: WARNER CHILCOTT DIV WARNER LAMBERT CO
Marketing Status:
Discontinued
Patent and Exclusivity Information
