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Allopurinol

NDC 50268-030, Allopurinol, tablet, from AvPAK.

Product NDC
50268-030
Status
Listed
Labeler
AvPAK
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/50268-030 \
  -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
50268-030-1050268003010100 BLISTER PACK in 1 BOX (50268-030-10) / 1 TABLET in 1 BLISTER PACK (50268-030-11)

Linked data

RxNorm, label and prices

RxNorm concepts

RxNorm links no concept to this product's packages.

Related lookups

  • FDA label sections

    GET /v1/drugs/labels/5d330416-4289-762e-e063-6294a90a532e

Use it

Look up 50268-030 from code or an agent

curl
curl https://api.healthcare.dev/v1/drugs/ndc/50268-030 \
  -H "Authorization: Bearer $HDEV_API_KEY"
MCP prompt
Using the healthcare.dev MCP server, look up NDC 50268-030. 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.