Iomeron

Product NDC
0270-7250
11-digit product format
002707250
Labeler code
0270
Product ID
0270-7250_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
510 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
IOMEPROL510 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
0270-7250-10Iomeron56 in 1 BOXINJECTION, SOLUTION565
0270-7250-10Iomeron100 mL in 1 BOTTLE, GLASSINJECTION, SOLUTION1005

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDCDashboard titleSPL versionValidationDashboard ZIP
0270-7250IOMERON (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
0270-7250-100027072501056 BOTTLE, GLASS in 1 BOX (0270-7250-10) / 100 mL in 1 BOTTLE, GLASS2022-07-012027-02-01NoNoCurrent