NDC 0407-0778-02 - HYPAQUE

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: 0407-0778
Requested NDC: 0407-0778-02
Package NDCs from labels: 0407-0778-02
Manufacturer: Amersham Health Inc.
Effective date: 2006-04-13
Current FDA listing: Not matched in FDA.report NDC product tables

DailyMed Labels#

Label, Manufacturer, Effective date table
Label	Manufacturer	Effective date	Type
HYPAQUE - Amersham Health Inc.	Amersham Health Inc.	2006-04-13	HUMAN PRESCRIPTION DRUG LABELING

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDC	Product	Description	Form	Quantity	Strength	SPL version
0407-0778-02	HYPAQUE	200 mL in 1 BOTTLE	INJECTION, SOLUTION	200		1
0407-0778-02	HYPAQUE	10 in 1 BOX	INJECTION, SOLUTION	10		1

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDC	Dashboard title	SPL version	Validation	Dashboard ZIP
0407-0778	HYPAQUE (DIATRIZOATE MEGLUMINE AND DIATRIZOATE SODIUM) INJECTION, SOLUTION [AMERSHAM HEALTH INC.]	1	2 package rows	20060525_0AAAA03E-B258-45EC-89C8-06E1353F57EF.zip

DailyMed Socrata Ingredients#

Ingredient, Type, UNII table
Ingredient	Type	UNII	DailyMed label	SPL version
Diatrizoate Meglumine	ACTIVE INGREDIENT	3X9MR4N98U	HYPAQUE (DIATRIZOATE MEGLUMINE AND DIATRIZOATE SODIUM) INJECTION, SOLUTION [AMERSHAM HEALTH INC.]	1
Diatrizoate Sodium	ACTIVE INGREDIENT	V5403H8VG7	HYPAQUE (DIATRIZOATE MEGLUMINE AND DIATRIZOATE SODIUM) INJECTION, SOLUTION [AMERSHAM HEALTH INC.]	1
Diatrizoate	ACTIVE MOIETY		HYPAQUE (DIATRIZOATE MEGLUMINE AND DIATRIZOATE SODIUM) INJECTION, SOLUTION [AMERSHAM HEALTH INC.]	1
Iodine	INACTIVE INGREDIENT	9679TC07X4	HYPAQUE (DIATRIZOATE MEGLUMINE AND DIATRIZOATE SODIUM) INJECTION, SOLUTION [AMERSHAM HEALTH 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
0AAAA03E-B258-45EC-89C8-06E1353F57EF			0AAAA03E-B258-45EC-89C8-06E1353F57EF	2006-04-13	Warnings, Adverse reactions	Exact identifier spl id: 0AAAA03E-B258-45EC-89C8-06E1353F57EF spl set id: 0AAAA03E-B258-45EC-89C8-06E1353F57EF

Reported adverse events (FAERS/openFDA)#

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