NDC 0469-7271-01 - 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: 0469-7271
Requested NDC: 0469-7271-01
Package NDCs from labels: 0469-7271-01
Manufacturer: Fujisawa Healthcare, Inc.
Effective date: 2006-06-08
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 FOR INJECTION, USP)	Fujisawa Healthcare, Inc.	2006-06-08	Human prescription drug label

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDC	Product	Description	Form	Quantity	Strength	SPL version
0469-7271-01	Cefizox	1 in 1 VIAL	INJECTION, POWDER, LYOPHILIZED,	1		1
0469-7271-01	Cefizox	10 in 1 PACKAGE	INJECTION, POWDER, LYOPHILIZED,	10		1

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDC	Dashboard title	SPL version	Validation	Dashboard ZIP
0469-7271	CEFIZOX (CEFTIZOXIME) INJECTION, POWDER, LYOPHILIZED, FOR SOLUTION [FUJISAWA HEALTHCARE, INC.]	1	2 package rows	20060828_0013824B-6AEE-4DA4-AFFD-35BC6BF19D91.zip

DailyMed Socrata Ingredients#

Ingredient, Type, UNII table
Ingredient	Type	UNII	DailyMed label	SPL version	Uploaded
ceftizoxime sodium	ACTIVE INGREDIENT	26337D5X88	CEFIZOX (CEFTIZOXIME) INJECTION, POWDER, LYOPHILIZED, FOR SOLUTION [FUJISAWA HEALTHCARE, INC.]	1
ceftizoxime	ACTIVE MOIETY	C43C467DPE	CEFIZOX (CEFTIZOXIME) INJECTION, POWDER, LYOPHILIZED, FOR SOLUTION [FUJISAWA HEALTHCARE, 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
0013824B-6AEE-4DA4-AFFD-35BC6BF19D91			0013824B-6AEE-4DA4-AFFD-35BC6BF19D91	2006-06-08	Warnings, Adverse reactions	Exact identifier spl id: 0013824B-6AEE-4DA4-AFFD-35BC6BF19D91 spl set id: 0013824B-6AEE-4DA4-AFFD-35BC6BF19D91

Reported adverse events (FAERS/openFDA)#

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