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LEVOTHYROXINE SODIUM

NDC 70518-4435, LEVOTHYROXINE SODIUM, tablet, from REMEDYREPACK INC..

Product NDC
70518-4435
Status
Listed
Labeler
REMEDYREPACK INC.
Dosage form
TABLET
Route
ORAL
Product type
HUMAN PRESCRIPTION DRUG
Marketing category
ANDA
Application
ANDA211417
DEA schedule
None
Request
curl https://api.healthcare.dev/v1/drugs/ndc/70518-4435 \
  -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
70518-4435-07051844350090 TABLET in 1 BOTTLE (70518-4435-0)

Linked data

RxNorm, label and prices

RxNorm concepts

Related lookups

  • FDA label sections

    GET /v1/drugs/labels/9ad82faf-3734-42a1-befe-f6197b27f534

Use it

Look up 70518-4435 from code or an agent

curl
curl https://api.healthcare.dev/v1/drugs/ndc/70518-4435 \
  -H "Authorization: Bearer $HDEV_API_KEY"
MCP prompt
Using the healthcare.dev MCP server, look up NDC 70518-4435. 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.