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Floxuridine

NDC 0143-9270, Floxuridine, injection, powder, lyophilized, for solution, from Hikma Pharmaceuticals USA Inc..

Product NDC
0143-9270
Status
Listed
Labeler
Hikma Pharmaceuticals USA Inc.
Dosage form
INJECTION, POWDER, LYOPHILIZED, FOR SOLUTION
Route
INTRA-ARTERIAL
Product type
HUMAN PRESCRIPTION DRUG
Marketing category
ANDA
Application
ANDA075387
DEA schedule
None
Request
curl https://api.healthcare.dev/v1/drugs/ndc/0143-9270 \
  -H "Authorization: Bearer $HDEV_API_KEY"

Product

Active ingredients and packages

Active ingredients

  • FLOXURIDINE100 mg/mL

Pharmacologic classes

Antimetabolite [EPC]; Deoxyuridine [CS]

Package NDCNDC-11Package
0143-9270-01001439270011 VIAL in 1 BOX, UNIT-DOSE (0143-9270-01) / 5 mL in 1 VIAL

Linked data

RxNorm, label and prices

RxNorm concepts

Related lookups

  • FDA label sections

    GET /v1/drugs/labels/e3c2e3e7-bc83-465d-b615-3ad56580b3a7

Use it

Look up 0143-9270 from code or an agent

curl
curl https://api.healthcare.dev/v1/drugs/ndc/0143-9270 \
  -H "Authorization: Bearer $HDEV_API_KEY"
MCP prompt
Using the healthcare.dev MCP server, look up NDC 0143-9270. Tell me the product, its labeler, dosage form and route, its packages, and the RxNorm concepts it maps to.

Source: FDA, release 2026-10-23. Public domain. Reference data, not medical advice.