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Levothyroxine Sodium

NDC 70518-4390, Levothyroxine Sodium, tablet, from REMEDYREPACK INC..

Product NDC
70518-4390
Status
Listed
Labeler
REMEDYREPACK INC.
Dosage form
TABLET
Route
ORAL
Product type
HUMAN PRESCRIPTION DRUG
Marketing category
ANDA
Application
ANDA209713
DEA schedule
None
Request
curl https://api.healthcare.dev/v1/drugs/ndc/70518-4390 \
  -H "Authorization: Bearer $HDEV_API_KEY"

Product

Active ingredients and packages

Active ingredients

  • LEVOTHYROXINE SODIUM.05 mg/1

Pharmacologic classes

Thyroxine [CS]; l-Thyroxine [EPC]

Package NDCNDC-11Package
70518-4390-07051843900090 TABLET in 1 BOTTLE (70518-4390-0)

Linked data

RxNorm, label and prices

RxNorm concepts

Related lookups

  • FDA label sections

    GET /v1/drugs/labels/13e03769-9a4f-497f-9afa-95bf525090b3

Use it

Look up 70518-4390 from code or an agent

curl
curl https://api.healthcare.dev/v1/drugs/ndc/70518-4390 \
  -H "Authorization: Bearer $HDEV_API_KEY"
MCP prompt
Using the healthcare.dev MCP server, look up NDC 70518-4390. 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.