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Floxuridine

NDC 81643-9270, Floxuridine, injection, powder, lyophilized, for solution, from JND Therapeutics, Inc..

Product NDC
81643-9270
Status
Listed
Labeler
JND Therapeutics, 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/81643-9270 \
  -H "Authorization: Bearer $HDEV_API_KEY"

Product

Active ingredients and packages

Active ingredients

  • FLOXURIDINE500 mg/1

Pharmacologic classes

Antimetabolite [EPC]; Deoxyuridine [CS]

Package NDCNDC-11Package
81643-9270-1816439270011 VIAL in 1 BOX, UNIT-DOSE (81643-9270-1) / 5 INJECTION, POWDER, LYOPHILIZED, FOR SOLUTION in 1 VIAL

Linked data

RxNorm, label and prices

RxNorm concepts

Related lookups

  • FDA label sections

    GET /v1/drugs/labels/4681f23e-6b5e-433b-b245-3d0b4e64ebb2

  • Medicare Part B payment limits (ASP)

    GET /v1/drugs/asp?ndc=81643-9270

Use it

Look up 81643-9270 from code or an agent

curl
curl https://api.healthcare.dev/v1/drugs/ndc/81643-9270 \
  -H "Authorization: Bearer $HDEV_API_KEY"
MCP prompt
Using the healthcare.dev MCP server, look up NDC 81643-9270. 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.