Orange Book product

VORICONAZOLE 200MG/VIAL

Orange Book ANDA 220078 · ZHEJIANG NOVUS PHARMACEUTICALS CO LTD · Prescription

Key facts

Proprietary name VORICONAZOLE
Active ingredients VORICONAZOLE
Strength 200MG/VIAL
Dosage form POWDER
Route INTRAVENOUS
Application ANDA220078
Applicant holder ZHEJIANG NOVUS PHARMACEUTICALS CO LTD
Marketing status Prescription
Therapeutic equivalence (TE) code AP
Reference listed drug (RLD) No
Reference standard (RS) No
Approval date May 5, 2026

At a glance

  • 10–99 Marketed products with the same ingredient, strength and form
  • 1–9 Products in this application
  • No Reference listed drug

Counts are shown as ranges. Exact figures, trends and every underlying record are available in Orca1.

About Orange Book products

The FDA Orange Book lists approved drug products with their therapeutic equivalence (TE) codes, reference listed drugs and marketing status. Products approved before 1982 show an approval date of Jan 1, 1982.

Source: U.S. Food and Drug Administration (FDA), Approved Drug Products with Therapeutic Equivalence Evaluations (Orange Book)

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