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Liothyronine Sodium

NDC 71205-150, Liothyronine Sodium, tablet, from Proficient Rx LP.

Product NDC
71205-150
Status
Listed
Labeler
Proficient Rx LP
Dosage form
TABLET
Route
ORAL
Product type
HUMAN PRESCRIPTION DRUG
Marketing category
ANDA
Application
ANDA200295
DEA schedule
None
Request
curl https://api.healthcare.dev/v1/drugs/ndc/71205-150 \
  -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
71205-150-307120501503030 TABLET in 1 BOTTLE (71205-150-30)
71205-150-607120501506060 TABLET in 1 BOTTLE (71205-150-60)
71205-150-907120501509090 TABLET in 1 BOTTLE (71205-150-90)

Linked data

RxNorm, label and prices

RxNorm concepts

Related lookups

  • FDA label sections

    GET /v1/drugs/labels/f882d34f-6b9f-4d9d-8a3e-3054ba91c506

Use it

Look up 71205-150 from code or an agent

curl
curl https://api.healthcare.dev/v1/drugs/ndc/71205-150 \
  -H "Authorization: Bearer $HDEV_API_KEY"
MCP prompt
Using the healthcare.dev MCP server, look up NDC 71205-150. 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.