Home NDC 0270-7400 Iomeron
Product NDC 0270-7400
11-digit product format 002707400
Labeler code 0270
Product ID 0270-7400_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 816 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 Observed NDC auxiliary status history# This history shows the information present in each captured FDA auxiliary file. It is not a continuous regulatory timeline, and a missing record does not establish a status.
Historic NDC status page 1 of 1 · 6 matching rows.
View current auxiliary records. · View the auxiliary file history.
Captured / source date, Snapshot, Source SHA-256 table Captured / source date Snapshot Source SHA-256 2025-12-14 17:58 UTC · source 2025-12-05 d630ba8d3edf…732f749b63fb…2025-08-27 00:01 UTC · source 2025-08-26 f5e01cc5f278…a2eaf40c39c3…2025-04-01 02:39 UTC · source 2025-03-31 2ef7874e63bc…57b86245f4fa…2025-03-28 20:22 UTC · source 2025-03-28 a1b67e2a42f9…c4cf2c586c0d…2025-03-22 03:12 UTC · source 2025-03-21 cfe11265f3b6…090c488252e2…2025-03-10 12:48 UTC · source 2025-03-10 cdf11ea48f46…ba0047e9e063…
Additional Listing Data#
Finished product Yes
Brand name base Iomeron
Listing expiration 2026-12-31 Active Ingredients# Ingredient, Strength table Ingredient Strength IOMEPROL 816 mg/mL
Harmonized UNII identifiers# UNII identifiers page 1 of 1 · 1 matching rows.
Identifier, FDA.report destination table Identifier FDA.report destination 17E17JBP8L Internal UNII lookup
Harmonized SPL set identifiers# SPL set identifiers page 1 of 1 · 1 matching rows.
DailyMed Product Concepts# DailyMed Package Descriptions# Package NDC, Product, Description table Package NDC Product Description Form Quantity Strength SPL version 0270-7400-10 Iomeron 10 in 1 BOX INJECTION, SOLUTION 10 5 0270-7400-10 Iomeron 100 mL in 1 BOTTLE, GLASS INJECTION, SOLUTION 100 5 0270-7400-13 Iomeron 56 in 1 BOX INJECTION, SOLUTION 56 5 0270-7400-13 Iomeron 100 mL in 1 BOTTLE, GLASS INJECTION, SOLUTION 100 5 0270-7400-16 Iomeron 100 in 1 BOX INJECTION, SOLUTION 100 5 0270-7400-16 Iomeron 100 mL in 1 BOTTLE, GLASS INJECTION, SOLUTION 100 5 0270-7400-20 Iomeron 200 mL in 1 BOTTLE, GLASS INJECTION, SOLUTION 200 5 0270-7400-20 Iomeron 30 in 1 BOX INJECTION, SOLUTION 30 5
DailyMed Dashboard NDC Coverage# NDC, Dashboard title, SPL version table NDC Dashboard title SPL version Validation Dashboard ZIP 0270-7400 IOMERON (IOMEPROL INJECTION) INJECTION, SOLUTION [BRACCO DIAGNOSTICS INC] 4 Current NDC, Legacy NDC, 8 package rows 20241215_4b31d479-fd1c-5ed7-5bdf-dfd34fe08d98.zip
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.
Packages# Package NDC, 11-digit format, Description table Package NDC 11-digit format Description Marketing start Marketing end Sample Exclude flag Status 0270-7400-10 00270740010 10 BOTTLE, GLASS in 1 BOX (0270-7400-10) > 100 mL in 1 BOTTLE, GLASS 2022-07-01 0000-00-00 No No Current 0270-7400-13 00270740013 56 BOTTLE, GLASS in 1 BOX (0270-7400-13) / 100 mL in 1 BOTTLE, GLASS 2022-07-01 2026-09-01 No No Current 0270-7400-16 00270740016 100 BOTTLE, GLASS in 1 BOX (0270-7400-16) / 100 mL in 1 BOTTLE, GLASS 2022-07-01 2027-01-01 No No Current 0270-7400-20 00270740020 30 BOTTLE, GLASS in 1 BOX (0270-7400-20) / 200 mL in 1 BOTTLE, GLASS 2022-07-01 2027-02-01 No No Current