NDC 62157-925-01 - Nitazoxanide

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: 62157-925
Requested NDC: 62157-925-01
Package NDCs from labels: 62157-925-01
Manufacturer: AX Pharmaceutical Corp
Effective date: 2019-10-23
Current FDA listing: Not matched in FDA.report NDC product tables

DailyMed Labels#

Label, Manufacturer, Effective date table
Label	Manufacturer	Effective date	Type
Nitazoxanide - AX Pharmaceutical Corp	AX Pharmaceutical Corp	2019-10-23	BULK INGREDIENT

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	Exact identifier unii: SOA12P041N
Nitazoxanide	NITAZOXANIDE	Camber Pharmaceuticals, Inc.	295011e1-f919-4e5a-b9e7-4c784f623a86	2025-12-30	Adverse reactions	Exact identifier unii: SOA12P041N
Nitazoxanide	NITAZOXANIDE	Rising Pharma Holdings, Inc.	c0dc0656-3c46-43f9-adea-5285c522cef8	2025-10-09	Adverse reactions	Exact identifier unii: SOA12P041N
Nitazoxanide	NITAZOXANIDE	ANI Pharmaceuticals, Inc.	cd3652fa-a183-4fb6-9a21-73fbeba6fc4b	2025-03-05	Adverse reactions	Exact identifier unii: SOA12P041N

Reported adverse events (FAERS/openFDA)#

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