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LEVOTHYROXINE SODIUM

NDC 70710-1833, levothyroxine sodium, injection, powder, lyophilized, for solution, from Zydus Pharmaceuticals USA Inc..

Product NDC
70710-1833
Status
Listed
Labeler
Zydus Pharmaceuticals USA Inc.
Dosage form
INJECTION, POWDER, LYOPHILIZED, FOR SOLUTION
Route
INTRAVENOUS
Product type
HUMAN PRESCRIPTION DRUG
Marketing category
ANDA
Application
ANDA217066
DEA schedule
None
Request
curl https://api.healthcare.dev/v1/drugs/ndc/70710-1833 \
  -H "Authorization: Bearer $HDEV_API_KEY"

Product

Active ingredients and packages

Active ingredients

  • LEVOTHYROXINE SODIUM ANHYDROUS100 ug/5mL

Pharmacologic classes

Thyroxine [CS]; l-Thyroxine [EPC]

Package NDCNDC-11Package
70710-1833-1707101833011 VIAL, SINGLE-DOSE in 1 CARTON (70710-1833-1) / 5 mL in 1 VIAL, SINGLE-DOSE

Linked data

RxNorm, label and prices

RxNorm concepts

Related lookups

  • FDA label sections

    GET /v1/drugs/labels/bf8a952c-f05b-4814-b55a-ed04be015269

  • Medicare Part B payment limits (ASP)

    GET /v1/drugs/asp?ndc=70710-1833

Use it

Look up 70710-1833 from code or an agent

curl
curl https://api.healthcare.dev/v1/drugs/ndc/70710-1833 \
  -H "Authorization: Bearer $HDEV_API_KEY"
MCP prompt
Using the healthcare.dev MCP server, look up NDC 70710-1833. 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.