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Liothyronine sodium

NDC 16714-168, Liothyronine sodium, tablet, from Northstar Rx LLC.

Product NDC
16714-168
Status
Listed
Labeler
Northstar Rx LLC
Dosage form
TABLET
Route
ORAL
Product type
HUMAN PRESCRIPTION DRUG
Marketing category
ANDA
Application
ANDA214803
DEA schedule
None
Request
curl https://api.healthcare.dev/v1/drugs/ndc/16714-168 \
  -H "Authorization: Bearer $HDEV_API_KEY"

Product

Active ingredients and packages

Active ingredients

  • LIOTHYRONINE SODIUM50 ug/1

Pharmacologic classes

Triiodothyronine [CS]; l-Triiodothyronine [EPC]

Package NDCNDC-11Package
16714-168-0116714016801100 TABLET in 1 BOTTLE (16714-168-01)

Linked data

RxNorm, label and prices

RxNorm concepts

Related lookups

  • FDA label sections

    GET /v1/drugs/labels/c97dc9ec-af73-4836-aa0d-c27e66e792a9

  • NADAC price for package 16714016801

    GET /v1/drugs/nadac/16714016801

Use it

Look up 16714-168 from code or an agent

curl
curl https://api.healthcare.dev/v1/drugs/ndc/16714-168 \
  -H "Authorization: Bearer $HDEV_API_KEY"
MCP prompt
Using the healthcare.dev MCP server, look up NDC 16714-168. 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.