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Levothyroxine Sodium

NDC 24201-002, LEVOTHYROXINE SODIUM, injection, solution, from Hikma Pharmaceuticals USA Inc..

Product NDC
24201-002
Status
Listed
Labeler
Hikma Pharmaceuticals USA Inc.
Dosage form
INJECTION, SOLUTION
Route
INTRAVENOUS
Product type
HUMAN PRESCRIPTION DRUG
Marketing category
NDA
Application
NDA214253
DEA schedule
None
Request
curl https://api.healthcare.dev/v1/drugs/ndc/24201-002 \
  -H "Authorization: Bearer $HDEV_API_KEY"

Product

Active ingredients and packages

Active ingredients

  • LEVOTHYROXINE SODIUM100 ug/mL

Pharmacologic classes

Thyroxine [CS]; l-Thyroxine [EPC]

Package NDCNDC-11Package
24201-002-01242010002011 VIAL, SINGLE-DOSE in 1 CARTON (24201-002-01) / 2 mL in 1 VIAL, SINGLE-DOSE

Linked data

RxNorm, label and prices

RxNorm concepts

Related lookups

  • FDA label sections

    GET /v1/drugs/labels/6279390b-ee61-4ef9-ac15-25537ca783c1

  • Medicare Part B payment limits (ASP)

    GET /v1/drugs/asp?ndc=24201-002

Use it

Look up 24201-002 from code or an agent

curl
curl https://api.healthcare.dev/v1/drugs/ndc/24201-002 \
  -H "Authorization: Bearer $HDEV_API_KEY"
MCP prompt
Using the healthcare.dev MCP server, look up NDC 24201-002. 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.