FDA.reportPublic FDA data

NDC 0270-7017-24 - IOMERVU

This NDC is not currently matched to an FDA NDC product listing in FDA.report, but it is a valid NDC-form code. FDA.report is showing the available DailyMed label context for the product root.

Product NDC
0270-7017
Requested NDC
0270-7017-24
Package NDCs from labels
0270-7017-20, 0270-7017-21, 0270-7017-24, 0270-7017-25
Manufacturer
BRACCO DIAGNOSTICS INC | BIPSO GmbH | SPIN S.p.A. | BioChem Labor für biologishe und chemische Analytik GmbH
Effective date
2026-02-05
Current FDA listing
Not matched in FDA.report NDC product tables

DailyMed Labels#

Label, Manufacturer, Effective date table
LabelManufacturerEffective dateType
Iomeprol InjectionBRACCO DIAGNOSTICS INC | BIPSO GmbH | SPIN S.p.A. | BioChem Labor für biologishe und chemische Analytik GmbH2026-02-05HUMAN PRESCRIPTION DRUG LABEL

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDCProductDescriptionFormQuantityStrengthSPL version
0270-7017-20IOMERVU50 mL in 1 VIAL, GLASSINJECTION, SOLUTION504
0270-7017-20IOMERVU10 in 1 CASEINJECTION, SOLUTION104
0270-7017-21IOMERVU100 mL in 1 BOTTLE, GLASSINJECTION, SOLUTION1004
0270-7017-21IOMERVU10 in 1 CASEINJECTION, SOLUTION104
0270-7017-24IOMERVU10 in 1 CASEINJECTION, SOLUTION104
0270-7017-24IOMERVU150 mL in 1 BOTTLE, GLASSINJECTION, SOLUTION1504
0270-7017-25IOMERVU10 in 1 CASEINJECTION, SOLUTION104
0270-7017-25IOMERVU200 mL in 1 BOTTLE, GLASSINJECTION, SOLUTION2004

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 · 8 matching rows.

Brand, Generic, Manufacturer table
BrandGenericManufacturerSPL set IDEffective dateAvailable safety fieldsJoin
THAMTROMETHAMINEHospira, Inc.4af52118-c12b-4ad5-30bb-959848357e8a2026-05-27Warnings, Adverse reactionsExact identifier
unii: 023C2WHX2V
IOMERVUIOMEPROL INJECTIONBRACCO DIAGNOSTICS INCcb2e0e00-7c93-0fb4-89a5-861641662a5a2026-02-05Boxed warning, Warnings, Adverse reactionsExact identifier
application number: NDA216016
ndc (package): 0270-7017-24
ndc (package): 0270-7017-25
ndc (package): 0270-7018-28
ndc (package): 0270-7018-29
ndc (package): 0270-7017-21
ndc (package): 0270-7017-20
ndc (package): 0270-7018-26
ndc (package): 0270-7018-27
ndc (product): 0270-7017
ndc (product): 0270-7018
ndc11 (package): 00270701724
spl id: 50c571d8-759c-b711-b696-41c07a6ad82a
spl set id: cb2e0e00-7c93-0fb4-89a5-861641662a5a
unii: 17E17JBP8L
TromethamineTROMETHAMINEMILLA PHARMACEUTICALS INC.082b1104-502b-47af-95bf-0dbf2422990e2026-01-07Warnings, Adverse reactionsExact identifier
unii: 023C2WHX2V
IomeronIOMEPROL INJECTIONBRACCO DIAGNOSTICS INC4b31d479-fd1c-5ed7-5bdf-dfd34fe08d982025-11-19Exact identifier
unii: 17E17JBP8L
IomeronIOMEPROL INJECTIONBIPSO GmbH30a993a8-9afb-42c2-a4b2-72a6b361d43c2025-11-19Exact identifier
unii: 17E17JBP8L
TROMETHAMINETROMETHAMINEB. Braun Medical Inc.57db5686-7f7f-4999-87e3-e1cbbda4a98d2024-12-23Warnings, Adverse reactionsExact identifier
unii: 023C2WHX2V
AnubisMedSPF 50 BROAD SPECTRUM PROTECTION FLUID EMULSIONANUBIS COSMETICS SLe99d92c4-8768-9c0a-e053-2a95a90a609e2023-09-05WarningsExact identifier
unii: 023C2WHX2V
Anubis Barcelona Protective LineETHYLHEXYL METHOXYCINNAMATE, BUTYL METHOXYDIBENZOYLMETHANE, ETHYLHEXYL SALICYLATE, OCTOCRYLENEANUBIS COSMETICS SLec83846f-11c0-8f59-e053-2995a90ab9d22023-09-01WarningsExact identifier
unii: 023C2WHX2V

Reported adverse events (FAERS/openFDA)#

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