Home NDC 76381-735 Iomeron
Product NDC 76381-735
11-digit product format 763810735
Labeler code 76381
Product ID 76381-735_466579a4-4788-47ad-876a-b0a673f07a72
Type HUMAN PRESCRIPTION DRUG
Nonproprietary name Iomeprol Injection
Dosage form INJECTION, SOLUTION
Route INTRAVASCULAR
Labeler BIPSO GmbH
Marketing category UNAPPROVED DRUG FOR USE IN DRUG SHORTAGE
Marketing start 2022-07-01
Substance IOMEPROL
Active strength 714 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 Ingredient Strength IOMEPROL 714 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 76381-735-10 Iomeron 100 mL in 1 BOTTLE, GLASS INJECTION, SOLUTION 100 5 76381-735-10 Iomeron 56 in 1 BOX INJECTION, SOLUTION 56 5 76381-735-15 Iomeron 150 mL in 1 BOTTLE, GLASS INJECTION, SOLUTION 150 5 76381-735-15 Iomeron 30 in 1 BOX INJECTION, SOLUTION 30 5 76381-735-20 Iomeron 200 mL in 1 BOTTLE, GLASS INJECTION, SOLUTION 200 5 76381-735-20 Iomeron 10 in 1 BOX INJECTION, SOLUTION 10 5
DailyMed Dashboard NDC Coverage# NDC, Dashboard title, SPL version table NDC Dashboard title SPL version Validation Dashboard ZIP 76381-735 IOMERON (IOMEPROL INJECTION) INJECTION, SOLUTION [BIPSO GMBH] 4 Current NDC, Legacy NDC, 6 package rows 20241215_30a993a8-9afb-42c2-a4b2-72a6b361d43c.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 76381-735-10 76381073510 56 BOTTLE, GLASS in 1 BOX (76381-735-10) / 100 mL in 1 BOTTLE, GLASS 2022-07-01 2026-09-01 No No Current 76381-735-15 76381073515 30 BOTTLE, GLASS in 1 BOX (76381-735-15) / 150 mL in 1 BOTTLE, GLASS 2022-07-01 2027-02-01 No No Current 76381-735-20 76381073520 10 BOTTLE, GLASS in 1 BOX (76381-735-20) / 200 mL in 1 BOTTLE, GLASS 2022-07-01 2027-03-01 No No Current