VORICONAZOLE
Summary
FDA approved VORICONAZOLE by ZHEJIANG NOVUS. ANDA (Generic) approval on 2026-05-05. POWDER, INTRAVENOUS.
Details
Source
Drug Approval
External ID
ANDA220078-1
Action Date
2026-05-05
Status
Approved
Category
drug
Product Code
ANDA (Generic)
Product Description
VORICONAZOLE, POWDER, INTRAVENOUS. Application: ANDA220078
Company
Context & Analysis
Frequently Asked Questions
How often does ZHEJIANG NOVUS have FDA actions?
This is the only FDA action we have on record for ZHEJIANG NOVUS in our database.
Where can I find the official FDA record?
The official record is available on FDA.gov. Search for "ANDA220078-1" on FDA.gov for the full record. You can also use the openFDA API to query this record programmatically.
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