sodium iodide i 123

Generic: sodium iodide i 123

Labeler: curium us llc
NDC Directory HUMAN PRESCRIPTION DRUG ANDA Inactive Finished

Drug Facts

Product Profile

Brand Name sodium iodide i 123
Generic Name sodium iodide i 123
Labeler curium us llc
Dosage Form CAPSULE, GELATIN COATED
Routes
ORAL
Active Ingredients

sodium iodide i-123 200 uCi/1

Manufacturer
Curium US LLC

Identifiers & Regulatory

Product NDC 69945-602
Product ID 69945-602_24b19127-9a67-0ddf-e063-6394a90ae0b5
Product Type HUMAN PRESCRIPTION DRUG
Marketing Category ANDA
Application Number ANDA071910
Listing Expiration 2026-12-31
Marketing Start 2007-04-11

Normalized Code Variants

Searchable formats for this product NDC code

Digits Only 69945602
Hyphenated Format 69945-602

Supplemental Identifiers

UNII
29UKX3A616

Packaging Origin

Original Packager
true

Resolved Product View

Precedence rule: structured NDC data is preferred, falling back to linked label metadata when unavailable. Source tags show the origin of each value.

Resolved Identity

Brand Name sodium iodide i 123 (source: ndc)
Generic Name sodium iodide i 123 (source: ndc)
Application Number ANDA071910 (source: ndc)
Routes
ORAL
source: ndc

Resolved Composition

Strengths
  • 200 uCi/1
source: ndc
Packaging
  • 1 BOTTLE in 1 CAN (69945-602-20) / 1 CAPSULE, GELATIN COATED in 1 BOTTLE
source: ndc

Packages (1)

Ingredients (1)

sodium iodide i-123 (200 uCi/1)

Linked Drug Pages (1)

Raw FDA Data

View complete raw FDA NDC JSON payload
{"route": ["ORAL"], "spl_id": "24b19127-9a67-0ddf-e063-6394a90ae0b5", "openfda": {"unii": ["29UKX3A616"], "spl_set_id": ["493fa2ab-4eb0-4434-9739-3079b2f0e272"], "manufacturer_name": ["Curium US LLC"], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "1 BOTTLE in 1 CAN (69945-602-20)  / 1 CAPSULE, GELATIN COATED in 1 BOTTLE", "package_ndc": "69945-602-20", "marketing_start_date": "20070411"}], "brand_name": "SODIUM IODIDE I 123", "product_id": "69945-602_24b19127-9a67-0ddf-e063-6394a90ae0b5", "dosage_form": "CAPSULE, GELATIN COATED", "product_ndc": "69945-602", "generic_name": "sodium iodide i 123", "labeler_name": "Curium US LLC", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "SODIUM IODIDE I 123", "active_ingredients": [{"name": "SODIUM IODIDE I-123", "strength": "200 uCi/1"}], "application_number": "ANDA071910", "marketing_category": "ANDA", "marketing_start_date": "20070411", "listing_expiration_date": "20261231"}