sodium iodide i-131

Generic: sodium iodide i-131

Labeler: radnostix, inc.
NDC Directory HUMAN PRESCRIPTION DRUG ANDA Inactive Finished

Drug Facts

Product Profile

Brand Name sodium iodide i-131
Generic Name sodium iodide i-131
Labeler radnostix, inc.
Dosage Form KIT
Routes
ORAL
Manufacturer
Radnostix, Inc.

Identifiers & Regulatory

Product NDC 69208-000
Product ID 69208-000_490fdcc0-a035-b6f8-e063-6394a90a28a5
Product Type HUMAN PRESCRIPTION DRUG
Marketing Category ANDA
Application Number ANDA209166
Listing Expiration 2027-12-31
Marketing Start 2020-03-16

Normalized Code Variants

Searchable formats for this product NDC code

Digits Only 69208000
Hyphenated Format 69208-000

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-131 (source: ndc)
Generic Name sodium iodide i-131 (source: ndc)
Application Number ANDA209166 (source: ndc)
Routes
ORAL
source: ndc

Resolved Composition

Strengths
  • 3 ml
  • 300 mg
  • 1 ml
  • 2 ml
source: label
Packaging
  • 1 KIT in 1 BOX (69208-000-00) * 3 SOLUTION, CONCENTRATE in 1 VIAL, DISPENSING (69208-003-35) * 2 SOLUTION, CONCENTRATE in 1 VIAL, DISPENSING (69208-003-25) * 1 CARTON in 1 BOX / 2 BLISTER PACK in 1 CARTON / 10 CAPSULE in 1 BLISTER PACK * 1 SOLUTION, CONCENTRATE in 1 VIAL, DISPENSING (69208-003-15)
source: ndc

Packages (1)

69208-000-00 1 KIT in 1 BOX (69208-000-00) * 3 SOLUTION, CONCENTRATE in 1 VIAL, DISPENSING (69208-003-35) * 2 SOLUTION, CONCENTRATE in 1 VIAL, DISPENSING (69208-003-25) * 1 CARTON in 1 BOX / 2 BLISTER PACK in 1 CARTON / 10 CAPSULE in 1 BLISTER PACK * 1 SOLUTION, CONCENTRATE in 1 VIAL, DISPENSING (69208-003-15)

Ingredients (0)

No ingredient records.

Linked Drug Pages (1)

Sodium Iodide I-131 ndc-match (0.9)

Raw FDA Data

View complete raw FDA NDC JSON payload 
{"route": ["ORAL"], "spl_id": "490fdcc0-a035-b6f8-e063-6394a90a28a5", "openfda": {"spl_set_id": ["380e8e26-0625-4233-b36e-afb9f66e8a77"], "manufacturer_name": ["Radnostix, Inc."], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "1 KIT in 1 BOX (69208-000-00)  *  3 SOLUTION, CONCENTRATE in 1 VIAL, DISPENSING (69208-003-35)  *  2 SOLUTION, CONCENTRATE in 1 VIAL, DISPENSING (69208-003-25)  *  1 CARTON in 1 BOX / 2 BLISTER PACK in 1 CARTON / 10 CAPSULE in 1 BLISTER PACK *  1 SOLUTION, CONCENTRATE in 1 VIAL, DISPENSING (69208-003-15)", "package_ndc": "69208-000-00", "marketing_start_date": "20200316"}], "brand_name": "Sodium Iodide I-131", "product_id": "69208-000_490fdcc0-a035-b6f8-e063-6394a90a28a5", "dosage_form": "KIT", "product_ndc": "69208-000", "generic_name": "Sodium Iodide I-131", "labeler_name": "Radnostix, Inc.", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Sodium Iodide I-131", "application_number": "ANDA209166", "marketing_category": "ANDA", "marketing_start_date": "20200316", "listing_expiration_date": "20271231"}