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Cefotaxime

NDC 21586-012, cefotaxime injection, powder, for solution, from SteriMax Inc..

Product NDC
21586-012
Status
Listed
Labeler
SteriMax Inc.
Dosage form
POWDER, FOR SOLUTION
Route
INTRAMUSCULAR, INTRAVENOUS
Product type
HUMAN PRESCRIPTION DRUG
Marketing category
UNAPPROVED DRUG FOR USE IN DRUG SHORTAGE
Application
—
DEA schedule
None
Request
curl https://api.healthcare.dev/v1/drugs/ndc/21586-012 \
  -H "Authorization: Bearer $HDEV_API_KEY"

Product

Active ingredients and packages

Active ingredients

  • CEFOTAXIME SODIUM2 g/1

Pharmacologic classes

Cephalosporin Antibacterial [EPC]; Cephalosporins [CS]

Package NDCNDC-11Package
21586-012-022158600120210 VIAL in 1 PACKAGE (21586-012-02) / 1 POWDER, FOR SOLUTION in 1 VIAL (21586-012-01)

Linked data

RxNorm, label and prices

RxNorm concepts

Related lookups

  • FDA label sections

    GET /v1/drugs/labels/8efe3bd0-c43a-2bd6-e053-2a95a90a92fa

Use it

Look up 21586-012 from code or an agent

curl
curl https://api.healthcare.dev/v1/drugs/ndc/21586-012 \
  -H "Authorization: Bearer $HDEV_API_KEY"
MCP prompt
Using the healthcare.dev MCP server, look up NDC 21586-012. 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.