SODIUM IODIDE I 123

Product NDC
69945-602
11-digit product format
699450602
Labeler code
69945
Product ID
69945-602_24b19127-9a67-0ddf-e063-6394a90ae0b5
Type
HUMAN PRESCRIPTION DRUG
Nonproprietary name
sodium iodide i 123
Dosage form
CAPSULE, GELATIN COATED
Route
ORAL
Labeler
Curium US LLC
Application
ANDA071910
Marketing category
ANDA
Marketing start
2007-04-11
Substance
SODIUM IODIDE I-123
Active strength
200 uCi/1
NDC exclude flag
No
Listing certified through
2026-12-31
Current FDA listing
Yes

Additional Listing Data#

Finished product
Yes
Brand name base
SODIUM IODIDE I 123
Listing expiration
2026-12-31

Active Ingredients#

Ingredient, Strength table
IngredientStrength
SODIUM IODIDE I-123200 uCi/1

Harmonized Identifiers#

Field, Values table
FieldValues
Unii29UKX3A616

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDCProductDescriptionFormQuantityStrengthSPL version
69945-602-20SODIUM IODIDE I 1231 in 1 BOTTLECAPSULE, GELATIN COATED110
69945-602-20SODIUM IODIDE I 1231 in 1 CANCAPSULE, GELATIN COATED110

DailyMed Socrata Ingredients#

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDCDashboard titleSPL versionValidationDashboard ZIP
69945-602SODIUM IODIDE I 123 CAPSULE, GELATIN COATED [CURIUM US LLC]10Current NDC, Legacy NDC, 2 package rows20241019_493fa2ab-4eb0-4434-9739-3079b2f0e272.zip

Packages#

Package NDC, 11-digit format, Description table
Package NDC11-digit formatDescriptionUnitsMarketing startMarketing endSampleExclude flagStatus
69945-602-20699450602201 BOTTLE in 1 CAN (69945-602-20) / 1 CAPSULE, GELATIN COATED in 1 BOTTLE1 bottle2007-04-110000-00-00NoNoCurrent