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Sodium Iodide I-131

NDC 69208-000, Sodium Iodide I-131, kit, from Radnostix, Inc..

Product NDC
69208-000
Status
Listed
Labeler
Radnostix, Inc.
Dosage form
KIT
Route
ORAL
Product type
HUMAN PRESCRIPTION DRUG
Marketing category
ANDA
Application
ANDA209166
DEA schedule
None
Request
curl https://api.healthcare.dev/v1/drugs/ndc/69208-000 \
  -H "Authorization: Bearer $HDEV_API_KEY"

Product

Active ingredients and packages

Active ingredients

None listed.

Package NDCNDC-11Package
69208-000-00692080000001 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)

Linked data

RxNorm, label and prices

RxNorm concepts

RxNorm links no concept to this product's packages.

Related lookups

  • FDA label sections

    GET /v1/drugs/labels/380e8e26-0625-4233-b36e-afb9f66e8a77

Use it

Look up 69208-000 from code or an agent

curl
curl https://api.healthcare.dev/v1/drugs/ndc/69208-000 \
  -H "Authorization: Bearer $HDEV_API_KEY"
MCP prompt
Using the healthcare.dev MCP server, look up NDC 69208-000. Tell me the product, its labeler, dosage form and route, its packages, and the RxNorm concepts it maps to.
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Source: FDA, release 2026-10-23. Public domain. Reference data, not medical advice.