NDC 0469-7220-01 - Cefizox

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: 0469-7220
Requested NDC: 0469-7220-01
Package NDCs from labels: 0469-7220-01
Manufacturer: Astellas Pharma US, Inc.
Effective date: 2006-01-04
Current FDA listing: Not matched in FDA.report NDC product tables

DailyMed Labels#

Label, Manufacturer, Effective date table
Label	Manufacturer	Effective date	Type
CEFIZOX ® (ceftizoxime injection) IN GALAXY ® PLASTIC CONTAINER (PL2040)	Astellas Pharma US, Inc.	2006-01-04	Human prescription drug label

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDC	Product	Description	Form	Quantity	Strength	SPL version
0469-7220-01	Cefizox	50 mL in 1 BAG	SOLUTION	50		1

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDC	Dashboard title	SPL version	Validation	Dashboard ZIP
0469-7220	CEFIZOX (CEFTIZOXIME SODIUM) SOLUTION [ASTELLAS PHARMA US, INC.]	1	1 package rows	20060828_888998CC-C7F7-4F2A-8479-DF60F77BC2A1.zip

DailyMed Socrata Ingredients#

Ingredient, Type, UNII table
Ingredient	Type	UNII	DailyMed label	SPL version
Ceftizoxime Sodium	ACTIVE INGREDIENT	26337D5X88	CEFIZOX (CEFTIZOXIME SODIUM) SOLUTION [ASTELLAS PHARMA US, INC.]	1
Ceftizoxime	ACTIVE MOIETY	C43C467DPE	CEFIZOX (CEFTIZOXIME SODIUM) SOLUTION [ASTELLAS PHARMA US, INC.]	1
Dextrose hydrous	INACTIVE INGREDIENT	LX22YL083G	CEFIZOX (CEFTIZOXIME SODIUM) SOLUTION [ASTELLAS PHARMA US, INC.]	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 1 of 1 · 1 matching rows.

Brand, Generic, Manufacturer table
Brand	Generic	Manufacturer	SPL set ID	Effective date	Available safety fields	Join
A822E39E-6974-0F15-C0B9-EBE4CAFB4F8B			888998CC-C7F7-4F2A-8479-DF60F77BC2A1	2006-01-04	Warnings, Adverse reactions	Exact identifier spl id: A822E39E-6974-0F15-C0B9-EBE4CAFB4F8B spl set id: 888998CC-C7F7-4F2A-8479-DF60F77BC2A1

Reported adverse events (FAERS/openFDA)#

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