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Allopurinol

NDC 59651-285, Allopurinol, tablet, from Aurobindo Pharma Limited.

Product NDC
59651-285
Status
Listed
Labeler
Aurobindo Pharma Limited
Dosage form
TABLET
Route
ORAL
Product type
HUMAN PRESCRIPTION DRUG
Marketing category
ANDA
Application
ANDA215091
DEA schedule
None
Request
curl https://api.healthcare.dev/v1/drugs/ndc/59651-285 \
  -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
59651-285-0159651028501100 TABLET in 1 BOTTLE (59651-285-01)
59651-285-99596510285991000 TABLET in 1 BOTTLE (59651-285-99)

Linked data

RxNorm, label and prices

RxNorm concepts

Related lookups

  • FDA label sections

    GET /v1/drugs/labels/311ca755-c022-4251-97eb-dd9be86a993f

  • NADAC price for package 59651028501

    GET /v1/drugs/nadac/59651028501

  • NADAC price for package 59651028599

    GET /v1/drugs/nadac/59651028599

Use it

Look up 59651-285 from code or an agent

curl
curl https://api.healthcare.dev/v1/drugs/ndc/59651-285 \
  -H "Authorization: Bearer $HDEV_API_KEY"
MCP prompt
Using the healthcare.dev MCP server, look up NDC 59651-285. 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.