Iomeron

Product NDC
0270-9300
11-digit product format
002709300
Labeler code
0270
Product ID
0270-9300_18b52319-bd56-4fce-b6a4-358e3f8a3a04
Type
HUMAN PRESCRIPTION DRUG
Nonproprietary name
Iomeprol Injection
Dosage form
INJECTION, SOLUTION
Route
INTRAVASCULAR
Labeler
BRACCO DIAGNOSTICS INC
Marketing category
UNAPPROVED DRUG FOR USE IN DRUG SHORTAGE
Marketing start
2022-07-01
Substance
IOMEPROL
Active strength
612 mg/mL
Pharmacologic classes
Radiographic Contrast Agent [EPC], X-Ray Contrast Activity [MoA]
NDC exclude flag
No
Listing certified through
2026-12-31
Current FDA listing
Yes

Additional Listing Data#

Finished product
Yes
Brand name base
Iomeron
Listing expiration
2026-12-31

Active Ingredients#

Ingredient, Strength table
IngredientStrength
IOMEPROL612 mg/mL

Harmonized Identifiers#

Field, Values table
FieldValues
Unii17E17JBP8L

DailyMed Product Concepts#

Product concept, Relation, Version table
Product conceptRelationVersionEffective
77dc03a4-fbfc-e6a3-fe95-285bbae40d75Product name220250814

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDCProductDescriptionFormQuantityStrengthSPL version
0270-9300-06Iomeron500 mL in 1 BOTTLE, GLASSINJECTION, SOLUTION5005
0270-9300-06Iomeron6 in 1 BOXINJECTION, SOLUTION65

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDCDashboard titleSPL versionValidationDashboard ZIP
0270-9300IOMERON (IOMEPROL INJECTION) INJECTION, SOLUTION [BRACCO DIAGNOSTICS INC]4Current NDC, Legacy NDC, 2 package rows20241215_4b31d479-fd1c-5ed7-5bdf-dfd34fe08d98.zip

Packages#

Package NDC, 11-digit format, Description table
Package NDC11-digit formatDescriptionMarketing startMarketing endSampleExclude flagStatus
0270-9300-06002709300066 BOTTLE, GLASS in 1 BOX (0270-9300-06) / 500 mL in 1 BOTTLE, GLASS2022-07-012027-02-01NoNoCurrent