Iomeron

openFDA label record#

This page contains supplementary openFDA label data. For the canonical label presentation, use the corresponding DailyMed Structured Product Label.

Verified complete openFDA source JSON (canonical bytes are SHA-256 checked before publication)

Brand name
Iomeron
Generic name
IOMEPROL INJECTION
Manufacturer
BRACCO DIAGNOSTICS INC
Product type
HUMAN PRESCRIPTION DRUG
SPL set ID
4b31d479-fd1c-5ed7-5bdf-dfd34fe08d98
SPL ID
18b52319-bd56-4fce-b6a4-358e3f8a3a04
Version
5
Effective date
2025-11-19
Source export date
2026-11-06
Source partition
7
Source file
https://download.open.fda.gov/drug/label/drug-label-0007-of-0014.json.zip
Source object key
raw/openfda/drug-label/2026-11-06/90742968499056f8845d54427ea2950526b02c3f289aedd40679ed8e120a0e89/drug-label-0007-of-0014.json.zip
Source manifest SHA-256
8dff71fbef1291eb7711013e9a3a06194930757924a8946ae3034107a98d9463
Import run
20261106T075659Z
Imported at
2026-11-06 08:45:07
Harmonized routes table
Harmonized routes
INTRAVASCULAR

Reported adverse events (FAERS/openFDA)#

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