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Liothyronine sodium

NDC 68382-582, Liothyronine sodium, tablet, from Zydus Pharmaceuticals (USA) Inc..

Product NDC
68382-582
Status
Listed
Labeler
Zydus Pharmaceuticals (USA) Inc.
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/68382-582 \
  -H "Authorization: Bearer $HDEV_API_KEY"

Product

Active ingredients and packages

Active ingredients

  • LIOTHYRONINE SODIUM5 ug/1

Pharmacologic classes

Triiodothyronine [CS]; l-Triiodothyronine [EPC]

Package NDCNDC-11Package
68382-582-0168382058201100 TABLET in 1 BOTTLE (68382-582-01)
68382-582-10683820582101000 TABLET in 1 BOTTLE (68382-582-10)

Linked data

RxNorm, label and prices

RxNorm concepts

Related lookups

  • FDA label sections

    GET /v1/drugs/labels/c54cf95f-6465-4203-b98b-a54ba5a26843

  • NADAC price for package 68382058201

    GET /v1/drugs/nadac/68382058201

Use it

Look up 68382-582 from code or an agent

curl
curl https://api.healthcare.dev/v1/drugs/ndc/68382-582 \
  -H "Authorization: Bearer $HDEV_API_KEY"
MCP prompt
Using the healthcare.dev MCP server, look up NDC 68382-582. 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.