NDC 73377-025 - Voriconazole

This NDC is not currently matched to an FDA NDC product listing in FDA.report, but it is a valid NDC-form code. FDA.report is showing the available DailyMed label context for the product root.

Product NDC: 73377-025
Package NDCs from labels: 73377-025-01, 73377-025-02
Manufacturer: AX Pharmaceutical Corp
Effective date: 2024-10-21
Current FDA listing: Not matched in FDA.report NDC product tables

DailyMed Labels#

Label, Manufacturer, Effective date table
Label	Manufacturer	Effective date	Type
Voriconazole - AX Pharmaceutical Corp	AX Pharmaceutical Corp	2024-10-21	BULK INGREDIENT - ANIMAL DRUG

openFDA label cross-check#

OpenFDA label data provides additional search and identifier links. DailyMed’s Structured Product Label is the canonical label on FDA.report. Matching records are deduplicated before they are shown below.

Matched openFDA labels page 3 of 3 · 43 matching rows.

Brand, Generic, Manufacturer table
Brand	Generic	Manufacturer	SPL set ID	Effective date	Available safety fields	Join
voriconazole	VORICONAZOLE	Lupin Pharmaceuticals,Inc.	b4c934c0-c1bb-4b0a-bc32-fb9e77ef65fc	2024-01-31	Warnings, Adverse reactions	Exact identifier unii: JFU09I87TR
VORICONAZOLE	VORICONAZOLE	Novel Laboratories, Inc.	53ecce53-57b8-4af1-b4ac-7d37eb25711f	2023-12-05	Warnings, Adverse reactions	Exact identifier unii: JFU09I87TR
Voriconazole	VORICONAZOLE	Xellia Pharmaceuticals USA LLC	9ec6eda2-2f15-423b-9ec6-819379a426e1	2023-01-11	Warnings, Adverse reactions	Exact identifier unii: JFU09I87TR

Reported adverse events (FAERS/openFDA)#

Adverse event summaries are temporarily unavailable. Other product information remains available.