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Allopurinol

NDC 51655-782, allopurinol, tablet, from Northwind Health Company, LLC.

Product NDC
51655-782
Status
Listed
Labeler
Northwind Health Company, LLC
Dosage form
TABLET
Route
ORAL
Product type
HUMAN PRESCRIPTION DRUG
Marketing category
ANDA
Application
ANDA071587
DEA schedule
None
Request
curl https://api.healthcare.dev/v1/drugs/ndc/51655-782 \
  -H "Authorization: Bearer $HDEV_API_KEY"

Product

Active ingredients and packages

Active ingredients

  • ALLOPURINOL300 mg/1

Pharmacologic classes

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

Package NDCNDC-11Package
51655-782-265165507822690 TABLET in 1 BOTTLE, PLASTIC (51655-782-26)
51655-782-525165507825230 TABLET in 1 BOTTLE, PLASTIC (51655-782-52)

Linked data

RxNorm, label and prices

RxNorm concepts

Related lookups

  • FDA label sections

    GET /v1/drugs/labels/da814597-50e6-48fa-e053-2995a90ab21b

Use it

Look up 51655-782 from code or an agent

curl
curl https://api.healthcare.dev/v1/drugs/ndc/51655-782 \
  -H "Authorization: Bearer $HDEV_API_KEY"
MCP prompt
Using the healthcare.dev MCP server, look up NDC 51655-782. 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.