Active Ingredient: FOMEPIZOLE
Proprietary Name: ANTIZOL
Dosage Form; Route of Administration: INJECTABLE; INJECTION
Strength: 1.5GM/1.5ML (1GM/ML) **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons**
Reference Listed Drug: Yes
Reference Standard: No
TE Code:
Application Number: N020696
Product Number: 001
Approval Date: Dec 4, 1997
Applicant Holder Full Name: PAR PHARMACEUTICAL INC
Marketing Status:
Discontinued
Patent and Exclusivity Information
