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Febuxostat

NDC 47335-721, Febuxostat, tablet, film coated, from Sun Pharmaceutical Industries, Inc..

Product NDC
47335-721
Status
Listed
Labeler
Sun Pharmaceutical Industries, Inc.
Dosage form
TABLET, FILM COATED
Route
ORAL
Product type
HUMAN PRESCRIPTION DRUG
Marketing category
ANDA
Application
ANDA205467
DEA schedule
None
Request
curl https://api.healthcare.dev/v1/drugs/ndc/47335-721 \
  -H "Authorization: Bearer $HDEV_API_KEY"

Product

Active ingredients and packages

Active ingredients

  • FEBUXOSTAT40 mg/1

Pharmacologic classes

Xanthine Oxidase Inhibitor [EPC]; Xanthine Oxidase Inhibitors [MoA]

Package NDCNDC-11Package
47335-721-1347335072113500 TABLET, FILM COATED in 1 BOTTLE (47335-721-13)
47335-721-814733507218190 TABLET, FILM COATED in 1 BOTTLE (47335-721-81)
47335-721-834733507218330 TABLET, FILM COATED in 1 BOTTLE (47335-721-83)

Linked data

RxNorm, label and prices

RxNorm concepts

Related lookups

  • FDA label sections

    GET /v1/drugs/labels/1f7541bd-bf32-422b-b99a-89193cf193ca

  • NADAC price for package 47335072183

    GET /v1/drugs/nadac/47335072183

Use it

Look up 47335-721 from code or an agent

curl
curl https://api.healthcare.dev/v1/drugs/ndc/47335-721 \
  -H "Authorization: Bearer $HDEV_API_KEY"
MCP prompt
Using the healthcare.dev MCP server, look up NDC 47335-721. 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.