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NDC 0074-7070, Levothyroxine Sodium, tablet, from AbbVie Inc..

Product NDC
0074-7070
Status
Listed
Labeler
AbbVie Inc.
Dosage form
TABLET
Route
ORAL
Product type
HUMAN PRESCRIPTION DRUG
Marketing category
NDA
Application
NDA021402
DEA schedule
None
Request
curl https://api.healthcare.dev/v1/drugs/ndc/0074-7070 \
  -H "Authorization: Bearer $HDEV_API_KEY"

Product

Active ingredients and packages

Active ingredients

  • LEVOTHYROXINE SODIUM175 ug/1

Pharmacologic classes

Thyroxine [CS]; l-Thyroxine [EPC]

Package NDCNDC-11Package
0074-7070-19000747070191000 TABLET in 1 BOTTLE (0074-7070-19)
0074-7070-900007470709090 TABLET in 1 BOTTLE (0074-7070-90)

Linked data

RxNorm, label and prices

RxNorm concepts

Related lookups

  • FDA label sections

    GET /v1/drugs/labels/1e11ad30-1041-4520-10b0-8f9d30d30fcc

  • NADAC price for package 00074707019

    GET /v1/drugs/nadac/00074707019

  • NADAC price for package 00074707090

    GET /v1/drugs/nadac/00074707090

Use it

Look up 0074-7070 from code or an agent

curl
curl https://api.healthcare.dev/v1/drugs/ndc/0074-7070 \
  -H "Authorization: Bearer $HDEV_API_KEY"
MCP prompt
Using the healthcare.dev MCP server, look up NDC 0074-7070. 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.