Active Ingredient: PHENYTOIN
Proprietary Name: PHENYTOIN
Dosage Form; Route of Administration: SUSPENSION; ORAL
Strength: 125MG/5ML
Reference Listed Drug: No
Reference Standard: No
TE Code:
Application Number: A040420
Product Number: 001
Approval Date: Apr 19, 2002
Applicant Holder Full Name: PAI HOLDINGS LLC DBA PHARMACEUTICAL ASSOCIATES INC
Marketing Status:
Discontinued
Patent and Exclusivity Information