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Orange Book: Approved Drug Products with Therapeutic Equivalence Evaluations

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Product Details for NDA 020696

ANTIZOL (FOMEPIZOLE)
1.5GM/1.5ML (1GM/ML) **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons**
Marketing Status: Discontinued
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Strength: 1.5GM/1.5ML (1GM/ML) **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons**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
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