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SSKI

NDC 71740-112, Potassium Iodide, solution, from Avondale Pharmaceuticals, LLC.

Product NDC
71740-112
Status
Listed
Labeler
Avondale Pharmaceuticals, LLC
Dosage form
SOLUTION
Route
ORAL
Product type
HUMAN PRESCRIPTION DRUG
Marketing category
UNAPPROVED DRUG OTHER
Application
—
DEA schedule
None
Request
curl https://api.healthcare.dev/v1/drugs/ndc/71740-112 \
  -H "Authorization: Bearer $HDEV_API_KEY"

Product

Active ingredients and packages

Active ingredients

  • POTASSIUM IODIDE1 g/mL
Package NDCNDC-11Package
71740-112-30717400112301 BOTTLE, WITH APPLICATOR in 1 CARTON (71740-112-30) / 30 mL in 1 BOTTLE, WITH APPLICATOR

Linked data

RxNorm, label and prices

RxNorm concepts

Related lookups

  • FDA label sections

    GET /v1/drugs/labels/ca1d3449-ea29-49a4-8863-365ec95f1553

Use it

Look up 71740-112 from code or an agent

curl
curl https://api.healthcare.dev/v1/drugs/ndc/71740-112 \
  -H "Authorization: Bearer $HDEV_API_KEY"
MCP prompt
Using the healthcare.dev MCP server, look up NDC 71740-112. 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.