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liothyronine sodium

NDC 62756-589, liothyronine sodium, tablet, from Sun Pharmaceutical Industries, Inc..

Product NDC
62756-589
Status
Listed
Labeler
Sun Pharmaceutical Industries, Inc.
Dosage form
TABLET
Route
ORAL
Product type
HUMAN PRESCRIPTION DRUG
Marketing category
ANDA
Application
ANDA091382
DEA schedule
None
Request
curl https://api.healthcare.dev/v1/drugs/ndc/62756-589 \
  -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
62756-589-016275605890190 TABLET in 1 BOTTLE (62756-589-01)
62756-589-0862756058908100 TABLET in 1 BOTTLE (62756-589-08)
62756-589-18627560589181000 TABLET in 1 BOTTLE (62756-589-18)
62756-589-836275605898330 TABLET in 1 BOTTLE (62756-589-83)
62756-589-8862756058988100 TABLET in 1 BOTTLE (62756-589-88)

Linked data

RxNorm, label and prices

RxNorm concepts

Related lookups

  • FDA label sections

    GET /v1/drugs/labels/892e63ef-3a60-45fa-b12b-d6795acc0956

  • NADAC price for package 62756058988

    GET /v1/drugs/nadac/62756058988

Use it

Look up 62756-589 from code or an agent

curl
curl https://api.healthcare.dev/v1/drugs/ndc/62756-589 \
  -H "Authorization: Bearer $HDEV_API_KEY"
MCP prompt
Using the healthcare.dev MCP server, look up NDC 62756-589. 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.