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Levothyroxine Sodium

NDC 71205-655, Levothyroxine Sodium, tablet, from Proficient Rx LP.

Product NDC
71205-655
Status
Listed
Labeler
Proficient Rx LP
Dosage form
TABLET
Route
ORAL
Product type
HUMAN PRESCRIPTION DRUG
Marketing category
NDA AUTHORIZED GENERIC
Application
NDA021342
DEA schedule
None
Request
curl https://api.healthcare.dev/v1/drugs/ndc/71205-655 \
  -H "Authorization: Bearer $HDEV_API_KEY"

Product

Active ingredients and packages

Active ingredients

  • LEVOTHYROXINE SODIUM75 ug/1

Pharmacologic classes

Thyroxine [CS]; l-Thyroxine [EPC]

Package NDCNDC-11Package
71205-655-307120506553030 TABLET in 1 BOTTLE (71205-655-30)
71205-655-607120506556060 TABLET in 1 BOTTLE (71205-655-60)
71205-655-907120506559090 TABLET in 1 BOTTLE (71205-655-90)

Linked data

RxNorm, label and prices

RxNorm concepts

Related lookups

  • FDA label sections

    GET /v1/drugs/labels/ca197216-83f1-470a-9313-d1b923924661

Use it

Look up 71205-655 from code or an agent

curl
curl https://api.healthcare.dev/v1/drugs/ndc/71205-655 \
  -H "Authorization: Bearer $HDEV_API_KEY"
MCP prompt
Using the healthcare.dev MCP server, look up NDC 71205-655. 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.