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Allopurinol

NDC 16571-884, allopurinol, tablet, from Rising Pharma Holdings, Inc..

Product NDC
16571-884
Status
Listed
Labeler
Rising Pharma Holdings, Inc.
Dosage form
TABLET
Route
ORAL
Product type
HUMAN PRESCRIPTION DRUG
Marketing category
NDA AUTHORIZED GENERIC
Application
NDA016084
DEA schedule
None
Request
curl https://api.healthcare.dev/v1/drugs/ndc/16571-884 \
  -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
16571-884-0116571088401100 TABLET in 1 BOTTLE (16571-884-01)
16571-884-091657108840990 TABLET in 1 BOTTLE (16571-884-09)
16571-884-10165710884101000 TABLET in 1 BOTTLE (16571-884-10)
16571-884-5016571088450500 TABLET in 1 BOTTLE (16571-884-50)

Linked data

RxNorm, label and prices

RxNorm concepts

Related lookups

  • FDA label sections

    GET /v1/drugs/labels/30ad5ba2-1cef-4933-b104-0597f6a2aaa2

  • NADAC price for package 16571088409

    GET /v1/drugs/nadac/16571088409

Use it

Look up 16571-884 from code or an agent

curl
curl https://api.healthcare.dev/v1/drugs/ndc/16571-884 \
  -H "Authorization: Bearer $HDEV_API_KEY"
MCP prompt
Using the healthcare.dev MCP server, look up NDC 16571-884. 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.