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Cefoxitin

NDC 63323-342, Cefoxitin Sodium, powder, for solution, from Fresenius Kabi USA, LLC.

Product NDC
63323-342
Status
Listed
Labeler
Fresenius Kabi USA, LLC
Dosage form
POWDER, FOR SOLUTION
Route
INTRAVENOUS
Product type
HUMAN PRESCRIPTION DRUG
Marketing category
ANDA
Application
ANDA065414
DEA schedule
None
Request
curl https://api.healthcare.dev/v1/drugs/ndc/63323-342 \
  -H "Authorization: Bearer $HDEV_API_KEY"

Product

Active ingredients and packages

Active ingredients

  • CEFOXITIN SODIUM2 g/1

Pharmacologic classes

Cephalosporin Antibacterial [EPC]; Cephalosporins [CS]

Package NDCNDC-11Package
63323-342-256332303422525 VIAL in 1 CARTON (63323-342-25) / 1 POWDER, FOR SOLUTION in 1 VIAL (63323-342-01)
63323-342-296332303422925 VIAL in 1 CARTON (63323-342-29) / 1 POWDER, FOR SOLUTION in 1 VIAL (63323-342-41)

Linked data

RxNorm, label and prices

RxNorm concepts

Related lookups

  • FDA label sections

    GET /v1/drugs/labels?ndc=63323-342

  • Medicare Part B payment limits (ASP)

    GET /v1/drugs/asp?ndc=63323-342

Use it

Look up 63323-342 from code or an agent

curl
curl https://api.healthcare.dev/v1/drugs/ndc/63323-342 \
  -H "Authorization: Bearer $HDEV_API_KEY"
MCP prompt
Using the healthcare.dev MCP server, look up NDC 63323-342. 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.