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Levothyroxine Sodium

NDC 71205-237, Levothyroxine Sodium, tablet, from Proficient Rx LP.

Product NDC
71205-237
Status
Listed
Labeler
Proficient Rx LP
Dosage form
TABLET
Route
ORAL
Product type
HUMAN PRESCRIPTION DRUG
Marketing category
NDA
Application
NDA021210
DEA schedule
None
Request
curl https://api.healthcare.dev/v1/drugs/ndc/71205-237 \
  -H "Authorization: Bearer $HDEV_API_KEY"

Product

Active ingredients and packages

Active ingredients

  • LEVOTHYROXINE SODIUM.137 mg/1

Pharmacologic classes

Thyroxine [CS]; l-Thyroxine [EPC]

Package NDCNDC-11Package
71205-237-307120502373030 TABLET in 1 BOTTLE, PLASTIC (71205-237-30)
71205-237-607120502376060 TABLET in 1 BOTTLE, PLASTIC (71205-237-60)
71205-237-907120502379090 TABLET in 1 BOTTLE, PLASTIC (71205-237-90)

Linked data

RxNorm, label and prices

RxNorm concepts

Related lookups

  • FDA label sections

    GET /v1/drugs/labels/18c7c63a-642e-47fe-a8ee-12aaf652b2aa

Use it

Look up 71205-237 from code or an agent

curl
curl https://api.healthcare.dev/v1/drugs/ndc/71205-237 \
  -H "Authorization: Bearer $HDEV_API_KEY"
MCP prompt
Using the healthcare.dev MCP server, look up NDC 71205-237. Tell me the product, its labeler, dosage form and route, its packages, and the RxNorm concepts it maps to.

Source: FDA, release 2026-10-23. Public domain. Reference data, not medical advice.