Orange Book product · Brand (NDA)
IOMERVU
IOMEPROL
At a glance
Nov 27, 2024
Approved
Brand (NDA)
Application
Not listed
TE code
None
Listed patents
Key dates
Approval
FDA approval date of this drug product.
Nov 27, 2024
1 yr 7 mo ago
Today
Exclusivity ends · NCE
New chemical entity exclusivity (5 years)
Nov 27, 2029
in 3 yr 6 mo
Pharmaceutical detail
Active ingredient
IOMEPROL
Strength
15GM IODINE/50ML (300MG IODINE/ML)
Dosage form
SOLUTION
Route
INTRA-ARTERIAL
TE code
Not listed
Application
NDA 216016
Product number
002
Marketing status
DISCN
Reference listed drug (RLD)
Yes
Reference standard (RS)
No
Active-ingredient family
View full familyThis is a reference-listed drug (RLD) — the basis for generic (ANDA) applications. Other products sharing this ingredient are listed below.
Marketing exclusivity (1)
- NCENew chemical entity exclusivity (5 years)
Nov 27, 2029
in 3 yr 6 mo
Listed patents
No patents are listed against this product in the Orange Book. Listed patents reflect those the NDA holder submits under 21 U.S.C. 355 and are not exhaustive.
