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Cefuroxime sodium

NDC 25021-119, Cefuroxime sodium, injection, powder, for solution, from Sagent Pharmaceuticals.

Product NDC
25021-119
Status
Listed
Labeler
Sagent Pharmaceuticals
Dosage form
INJECTION, POWDER, FOR SOLUTION
Route
INTRAVENOUS
Product type
HUMAN PRESCRIPTION DRUG
Marketing category
ANDA
Application
ANDA064125
DEA schedule
None
Request
curl https://api.healthcare.dev/v1/drugs/ndc/25021-119 \
  -H "Authorization: Bearer $HDEV_API_KEY"

Product

Active ingredients and packages

Active ingredients

  • CEFUROXIME SODIUM1.5 g/20mL

Pharmacologic classes

Cephalosporin Antibacterial [EPC]; Cephalosporins [CS]

Package NDCNDC-11Package
25021-119-202502101192025 VIAL in 1 CARTON (25021-119-20) / 20 mL in 1 VIAL

Linked data

RxNorm, label and prices

RxNorm concepts

Related lookups

  • FDA label sections

    GET /v1/drugs/labels/0a145288-733a-4966-b7ae-dc96eb103d8c

  • Medicare Part B payment limits (ASP)

    GET /v1/drugs/asp?ndc=25021-119

Use it

Look up 25021-119 from code or an agent

curl
curl https://api.healthcare.dev/v1/drugs/ndc/25021-119 \
  -H "Authorization: Bearer $HDEV_API_KEY"
MCP prompt
Using the healthcare.dev MCP server, look up NDC 25021-119. 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.