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levothyroxine sodium

NDC 71205-352, levothyroxine sodium, tablet, from Proficient Rx LP.

Product NDC
71205-352
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/71205-352 \
  -H "Authorization: Bearer $HDEV_API_KEY"

Product

Active ingredients and packages

Active ingredients

  • LEVOTHYROXINE SODIUM50 ug/1

Pharmacologic classes

Thyroxine [CS]; l-Thyroxine [EPC]

Package NDCNDC-11Package
71205-352-307120503523030 TABLET in 1 BOTTLE (71205-352-30)
71205-352-607120503526060 TABLET in 1 BOTTLE (71205-352-60)
71205-352-907120503529090 TABLET in 1 BOTTLE (71205-352-90)

Linked data

RxNorm, label and prices

RxNorm concepts

Related lookups

  • FDA label sections

    GET /v1/drugs/labels/3019762c-d480-4530-a3b2-762b523e7961

Use it

Look up 71205-352 from code or an agent

curl
curl https://api.healthcare.dev/v1/drugs/ndc/71205-352 \
  -H "Authorization: Bearer $HDEV_API_KEY"
MCP prompt
Using the healthcare.dev MCP server, look up NDC 71205-352. 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.