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Cefoxitin

NDC 0143-9878, Cefoxitin, injection, powder, for solution, from Hikma Pharmaceuticals USA Inc..

Product NDC
0143-9878
Status
Listed
Labeler
Hikma Pharmaceuticals USA Inc.
Dosage form
INJECTION, POWDER, FOR SOLUTION
Route
INTRAVENOUS
Product type
HUMAN PRESCRIPTION DRUG
Marketing category
ANDA
Application
ANDA065238
DEA schedule
None
Request
curl https://api.healthcare.dev/v1/drugs/ndc/0143-9878 \
  -H "Authorization: Bearer $HDEV_API_KEY"

Product

Active ingredients and packages

Active ingredients

  • CEFOXITIN SODIUM1 g/1

Pharmacologic classes

Cephalosporin Antibacterial [EPC]; Cephalosporins [CS]

Package NDCNDC-11Package
0143-9878-250014398782525 VIAL in 1 CARTON (0143-9878-25) / 1 INJECTION, POWDER, FOR SOLUTION in 1 VIAL (0143-9878-01)

Linked data

RxNorm, label and prices

RxNorm concepts

Related lookups

  • FDA label sections

    GET /v1/drugs/labels/d2c449b9-5624-4166-95b1-d7813b3d0445

  • Medicare Part B payment limits (ASP)

    GET /v1/drugs/asp?ndc=0143-9878

Use it

Look up 0143-9878 from code or an agent

curl
curl https://api.healthcare.dev/v1/drugs/ndc/0143-9878 \
  -H "Authorization: Bearer $HDEV_API_KEY"
MCP prompt
Using the healthcare.dev MCP server, look up NDC 0143-9878. 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.