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Orange Book: Approved Drug Products with Therapeutic Equivalence Evaluations

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Product Details for NDA 021630

VFEND (VORICONAZOLE)
200MG/5ML
Marketing Status: Prescription
Active Ingredient: VORICONAZOLE
Proprietary Name: VFEND
Dosage Form; Route of Administration: FOR SUSPENSION; ORAL
Strength: 200MG/5ML
Reference Listed Drug: Yes
Reference Standard: Yes
TE Code: AB
Application Number: N021630
Product Number: 001
Approval Date: Dec 19, 2003
Applicant Holder Full Name: PF PRISM CV
Marketing Status:  Prescription
Patent and Exclusivity Information
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