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Allopurinol

NDC 66267-665, allopurinol, tablet, from NuCare Pharmaceuticals, Inc..

Product NDC
66267-665
Status
Listed
Labeler
NuCare Pharmaceuticals, Inc.
Dosage form
TABLET
Route
ORAL
Product type
HUMAN PRESCRIPTION DRUG
Marketing category
ANDA
Application
ANDA203154
DEA schedule
None
Request
curl https://api.healthcare.dev/v1/drugs/ndc/66267-665 \
  -H "Authorization: Bearer $HDEV_API_KEY"

Product

Active ingredients and packages

Active ingredients

  • ALLOPURINOL100 mg/1

Pharmacologic classes

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

Package NDCNDC-11Package
66267-665-306626706653030 TABLET in 1 BOTTLE (66267-665-30)
66267-665-606626706656060 TABLET in 1 BOTTLE (66267-665-60)
66267-665-906626706659090 TABLET in 1 BOTTLE (66267-665-90)

Linked data

RxNorm, label and prices

RxNorm concepts

Related lookups

  • FDA label sections

    GET /v1/drugs/labels/44bcc8df-a803-010f-e054-00144ff88e88

Use it

Look up 66267-665 from code or an agent

curl
curl https://api.healthcare.dev/v1/drugs/ndc/66267-665 \
  -H "Authorization: Bearer $HDEV_API_KEY"
MCP prompt
Using the healthcare.dev MCP server, look up NDC 66267-665. 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.