Nitazoxanide

Manufacturer: AX Pharmaceutical Corp
Effective date: 2019-10-23
Label type: BULK INGREDIENT
Version: 1
Source: legacy-cache
Hydrated at: 2026-08-02 00:06:15

Label at a glance#

ProductNitazoxanide

Active ingredientNITAZOXANIDE

Label structure1 sections

Label contents#

Full prescribing information#

Nitazoxanide

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

image description

Products#

Every source-derived product name is available through these pages.

DailyMed product names page 1 of 1 · 1 matching rows.

Nitazoxanide

NDC Codes#

Product NDC, Package NDC table
Product NDC	Package NDC
62157-925	62157-925-01

Ingredients#

Every source-derived ingredient row is available through these pages.

DailyMed ingredient rows page 1 of 1 · 1 matching rows.

Name, UNII, Kind table
Name	UNII	Kind
NITAZOXANIDE	SOA12P041N	ACTIB

Source Document#

Source XML

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 1 of 1 · 4 matching rows.

Brand, Generic, Manufacturer table
Brand	Generic	Manufacturer	SPL set ID	Effective date	Available safety fields	Join
Nitazoxanide	NITAZOXANIDE	e5 Pharma, LLC	40a7cc30-76cd-49fe-965a-7823c4140d0f	2026-06-18	Adverse reactions	Name fallback brand name: Nitazoxanide generic name: NITAZOXANIDE
Nitazoxanide	NITAZOXANIDE	Camber Pharmaceuticals, Inc.	295011e1-f919-4e5a-b9e7-4c784f623a86	2025-12-30	Adverse reactions	Name fallback brand name: Nitazoxanide generic name: NITAZOXANIDE
Nitazoxanide	NITAZOXANIDE	Rising Pharma Holdings, Inc.	c0dc0656-3c46-43f9-adea-5285c522cef8	2025-10-09	Adverse reactions	Name fallback brand name: Nitazoxanide generic name: NITAZOXANIDE
Nitazoxanide	NITAZOXANIDE	ANI Pharmaceuticals, Inc.	cd3652fa-a183-4fb6-9a21-73fbeba6fc4b	2025-03-05	Adverse reactions	Name fallback brand name: Nitazoxanide generic name: NITAZOXANIDE

Reported adverse events (FAERS/openFDA)#

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