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Allopurinol

NDC 71921-241, Allopurinol, tablet, from Florida Pharmaceutical Products, LLC.

Product NDC
71921-241
Status
Listed
Labeler
Florida Pharmaceutical Products, LLC
Dosage form
TABLET
Route
ORAL
Product type
HUMAN PRESCRIPTION DRUG
Marketing category
ANDA
Application
ANDA204467
DEA schedule
None
Request
curl https://api.healthcare.dev/v1/drugs/ndc/71921-241 \
  -H "Authorization: Bearer $HDEV_API_KEY"

Product

Active ingredients and packages

Active ingredients

  • ALLOPURINOL200 mg/1

Pharmacologic classes

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

Package NDCNDC-11Package
71921-241-097192102410990 TABLET in 1 BOTTLE (71921-241-09)

Linked data

RxNorm, label and prices

RxNorm concepts

Related lookups

  • FDA label sections

    GET /v1/drugs/labels/815af471-5985-4819-936d-1f5f3d871ef8

  • NADAC price for package 71921024109

    GET /v1/drugs/nadac/71921024109

Use it

Look up 71921-241 from code or an agent

curl
curl https://api.healthcare.dev/v1/drugs/ndc/71921-241 \
  -H "Authorization: Bearer $HDEV_API_KEY"
MCP prompt
Using the healthcare.dev MCP server, look up NDC 71921-241. 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.