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liothyronine sodium

NDC 62756-591, liothyronine sodium, tablet, from Sun Pharmaceutical Industries, Inc..

Product NDC
62756-591
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/62756-591 \
  -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
62756-591-016275605910190 TABLET in 1 BOTTLE (62756-591-01)
62756-591-0862756059108100 TABLET in 1 BOTTLE (62756-591-08)
62756-591-18627560591181000 TABLET in 1 BOTTLE (62756-591-18)
62756-591-836275605918330 TABLET in 1 BOTTLE (62756-591-83)
62756-591-8862756059188100 TABLET in 1 BOTTLE (62756-591-88)

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 62756059188

    GET /v1/drugs/nadac/62756059188

Use it

Look up 62756-591 from code or an agent

curl
curl https://api.healthcare.dev/v1/drugs/ndc/62756-591 \
  -H "Authorization: Bearer $HDEV_API_KEY"
MCP prompt
Using the healthcare.dev MCP server, look up NDC 62756-591. 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.