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levothyroxine sodium

NDC 68071-5235, levothyroxine sodium, tablet, from NuCar Pharmaceuticals,Inc..

Product NDC
68071-5235
Status
Listed
Labeler
NuCar Pharmaceuticals,Inc.
Dosage form
TABLET
Route
ORAL
Product type
HUMAN PRESCRIPTION DRUG
Marketing category
NDA
Application
NDA021116
DEA schedule
None
Request
curl https://api.healthcare.dev/v1/drugs/ndc/68071-5235 \
  -H "Authorization: Bearer $HDEV_API_KEY"

Product

Active ingredients and packages

Active ingredients

  • LEVOTHYROXINE SODIUM100 ug/1

Pharmacologic classes

Thyroxine [CS]; l-Thyroxine [EPC]

Package NDCNDC-11Package
68071-5235-96807152350990 TABLET in 1 BOTTLE (68071-5235-9)

Linked data

RxNorm, label and prices

RxNorm concepts

Related lookups

  • FDA label sections

    GET /v1/drugs/labels/a2194c58-b755-e6b5-e053-2a95a90a36d4

Use it

Look up 68071-5235 from code or an agent

curl
curl https://api.healthcare.dev/v1/drugs/ndc/68071-5235 \
  -H "Authorization: Bearer $HDEV_API_KEY"
MCP prompt
Using the healthcare.dev MCP server, look up NDC 68071-5235. 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.