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Orange Book: Approved Drug Products with Therapeutic Equivalence Evaluations

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Product Details for NDA 021267

VFEND (VORICONAZOLE)
200MG/VIAL
Marketing Status: Prescription
Active Ingredient: VORICONAZOLE
Proprietary Name: VFEND
Dosage Form; Route of Administration: INJECTABLE; INTRAVENOUS
Strength: 200MG/VIAL
Reference Listed Drug: Yes
Reference Standard: Yes
TE Code: AP
Application Number: N021267
Product Number: 001
Approval Date: May 24, 2002
Applicant Holder Full Name: PF PRISM CV
Marketing Status:  Prescription
Patent and Exclusivity Information
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