NDC 0407-0747-02 - Hypaque Sodium

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: 0407-0747
Requested NDC: 0407-0747-02
Package NDCs from labels: 0407-0747-02
Manufacturer: Amersham Health Inc.
Effective date: 2007-08-03
Current FDA listing: Not matched in FDA.report NDC product tables

DailyMed Labels#

Label, Manufacturer, Effective date table
Label	Manufacturer	Effective date	Type
HYPAQUE ™ Meglumine (Diatrizoate Meglumine Injection, USP) 60%	Amersham Health Inc.	2007-08-03	HUMAN PRESCRIPTION DRUG LABELING

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDC	Product	Description	Form	Quantity	Strength	SPL version
0407-0747-02	Hypaque Sodium	10 in 1 BOX	INJECTION, SOLUTION	10		1
0407-0747-02	Hypaque Sodium	100 mL in 1 VIAL	INJECTION, SOLUTION	100		1

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDC	Dashboard title	SPL version	Validation	Dashboard ZIP
0407-0747	HYPAQUE SODIUM (DIATRIZOATE MEGLUMINE) INJECTION, SOLUTION [AMERSHAM HEALTH INC.]	1	2 package rows	20070808_A0B58C0C-D67A-4BA6-8D84-CCDC78F24634.zip

DailyMed Socrata Ingredients#

Ingredient, Type, UNII table
Ingredient	Type	UNII	DailyMed label	SPL version	Uploaded
Diatrizoate Meglumine	ACTIVE INGREDIENT	3X9MR4N98U	HYPAQUE SODIUM (DIATRIZOATE MEGLUMINE) INJECTION, SOLUTION [AMERSHAM HEALTH INC.]	1
diatrizoic acid	ACTIVE MOIETY	5UVC90J1LK	HYPAQUE SODIUM (DIATRIZOATE MEGLUMINE) 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
23DF6AB0-CDBC-9415-26B6-CB075042D30E			A0B58C0C-D67A-4BA6-8D84-CCDC78F24634	2007-08-03	Warnings, Adverse reactions	Exact identifier spl id: 23DF6AB0-CDBC-9415-26B6-CB075042D30E spl set id: A0B58C0C-D67A-4BA6-8D84-CCDC78F24634

Reported adverse events (FAERS/openFDA)#

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