NDC 73377-329 - Isoniazid

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: 73377-329
Package NDCs from labels: 73377-329-01
Manufacturer: AX Pharmaceutical Corp
Effective date: 2025-08-08
Current FDA listing: Not matched in FDA.report NDC product tables

DailyMed Labels#

Label, Manufacturer, Effective date table
Label	Manufacturer	Effective date	Type
Isoniazid - AX Pharmaceutical Corp	AX Pharmaceutical Corp	2025-08-08	BULK INGREDIENT - ANIMAL DRUG

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDC	Product	Description	Form	Quantity	Strength	SPL version
73377-329-01	Isoniazid	5000 g in 1 JAR	POWDER	5000		1

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 2 of 2 · 23 matching rows.

Brand, Generic, Manufacturer table
Brand	Generic	Manufacturer	SPL set ID	Effective date	Available safety fields	Join
Isoniazid	ISONIAZID	Teva Pharmaceuticals USA, Inc.	9499f1cf-2f46-4047-8b71-90aee7dee854	2021-10-31	Boxed warning, Warnings, Adverse reactions	Exact identifier unii: V83O1VOZ8L
Isoniazid	ISONIAZID	Aphena Pharma Solutions - Tennessee, LLC	cb6f5638-2d3a-4334-b272-6b4772d32d03	2020-03-23	Boxed warning, Warnings, Adverse reactions	Exact identifier unii: V83O1VOZ8L
Isoniazid	ISONIAZID	Proficient Rx LP	65e50989-d24c-4bb3-a041-d6aea2635ef1	2019-11-01	Boxed warning, Warnings, Adverse reactions	Exact identifier unii: V83O1VOZ8L

Reported adverse events (FAERS/openFDA)#

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