Orange Book product · Brand (NDA)
OPTIRAY 350
IOVERSOL
Brand (NDA)NDA 019710RX LIEBEL-FLARSHEIM
At a glance
Jan 22, 1992
Approved
Brand (NDA)
Application
Not listed
TE code
None
Listed patents
Key dates
Approval
FDA approval date of this drug product.
Jan 22, 1992
34 yr 11 mo ago
Today
Pharmaceutical detail
Active ingredient
IOVERSOL
Strength
74%
Dosage form
INJECTABLE
Route
INJECTION
TE code
Not listed
Application
NDA 019710
Product number
005
Marketing status
RX
Reference listed drug (RLD)
Yes
Reference standard (RS)
Yes
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.
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.
