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levothyroxine sodium

NDC 71205-351, levothyroxine sodium, tablet, from Proficient Rx LP.

Product NDC
71205-351
Status
Listed
Labeler
Proficient Rx LP
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/71205-351 \
  -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
71205-351-307120503513030 TABLET in 1 BOTTLE (71205-351-30)
71205-351-607120503516060 TABLET in 1 BOTTLE (71205-351-60)
71205-351-907120503519090 TABLET in 1 BOTTLE (71205-351-90)

Linked data

RxNorm, label and prices

RxNorm concepts

Related lookups

  • FDA label sections

    GET /v1/drugs/labels/12ccf2fd-ccf0-4bcf-8eee-e2a16c8b44d6

Use it

Look up 71205-351 from code or an agent

curl
curl https://api.healthcare.dev/v1/drugs/ndc/71205-351 \
  -H "Authorization: Bearer $HDEV_API_KEY"
MCP prompt
Using the healthcare.dev MCP server, look up NDC 71205-351. 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.