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Levothyroxine Sodium

NDC 59651-555, Levothyroxine Sodium, tablet, from Aurobindo Pharma Limited.

Product NDC
59651-555
Status
Listed
Labeler
Aurobindo Pharma Limited
Dosage form
TABLET
Route
ORAL
Product type
HUMAN PRESCRIPTION DRUG
Marketing category
ANDA
Application
ANDA216414
DEA schedule
None
Request
curl https://api.healthcare.dev/v1/drugs/ndc/59651-555 \
  -H "Authorization: Bearer $HDEV_API_KEY"

Product

Active ingredients and packages

Active ingredients

  • LEVOTHYROXINE SODIUM150 ug/1

Pharmacologic classes

Thyroxine [CS]; l-Thyroxine [EPC]

Package NDCNDC-11Package
59651-555-905965105559090 TABLET in 1 BOTTLE (59651-555-90)
59651-555-99596510555991000 TABLET in 1 BOTTLE (59651-555-99)

Linked data

RxNorm, label and prices

RxNorm concepts

Related lookups

  • FDA label sections

    GET /v1/drugs/labels/c760d0cc-2245-4914-8c67-d536c41ac90f

Use it

Look up 59651-555 from code or an agent

curl
curl https://api.healthcare.dev/v1/drugs/ndc/59651-555 \
  -H "Authorization: Bearer $HDEV_API_KEY"
MCP prompt
Using the healthcare.dev MCP server, look up NDC 59651-555. 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.