Orange Book product · Brand (NDA)
SODIUM IODIDE I 123
SODIUM IODIDE I-123
Brand (NDA)NDA 018671TE AARX CARDINAL HEALTH 418
At a glance
May 27, 1982
Approved
Brand (NDA)
Application
AA
TE code
None
Listed patents
Key dates
Approval
FDA approval date of this drug product.
May 27, 1982
44 yr 8 mo ago
Today
Pharmaceutical detail
Active ingredient
SODIUM IODIDE I-123
Strength
200uCi
Dosage form
CAPSULE
Route
ORAL
TE code
AA
Application
NDA 018671
Product number
002
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.
