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Cefotaxime

NDC 0143-9935, Cefotaxime, injection, from Hikma Pharmaceuticals USA Inc..

Product NDC
0143-9935
Status
Listed
Labeler
Hikma Pharmaceuticals USA Inc.
Dosage form
INJECTION
Route
INTRAVENOUS
Product type
HUMAN PRESCRIPTION DRUG
Marketing category
ANDA
Application
ANDA065071
DEA schedule
None
Request
curl https://api.healthcare.dev/v1/drugs/ndc/0143-9935 \
  -H "Authorization: Bearer $HDEV_API_KEY"

Product

Active ingredients and packages

Active ingredients

  • CEFOTAXIME SODIUM10 g/1

Pharmacologic classes

Cephalosporin Antibacterial [EPC]; Cephalosporins [CS]

Package NDCNDC-11Package
0143-9935-01001439935011 INJECTION in 1 PACKAGE (0143-9935-01)

Linked data

RxNorm, label and prices

RxNorm concepts

Related lookups

  • FDA label sections

    GET /v1/drugs/labels/ef1a6dc6-bc3d-4f09-8f92-7ff328f56561

Use it

Look up 0143-9935 from code or an agent

curl
curl https://api.healthcare.dev/v1/drugs/ndc/0143-9935 \
  -H "Authorization: Bearer $HDEV_API_KEY"
MCP prompt
Using the healthcare.dev MCP server, look up NDC 0143-9935. 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.