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Allopurinol

NDC 43063-935, Allopurinol, tablet, from PD-Rx Pharmaceuticals, Inc..

Product NDC
43063-935
Status
Listed
Labeler
PD-Rx Pharmaceuticals, Inc.
Dosage form
TABLET
Route
ORAL
Product type
HUMAN PRESCRIPTION DRUG
Marketing category
ANDA
Application
ANDA071450
DEA schedule
None
Request
curl https://api.healthcare.dev/v1/drugs/ndc/43063-935 \
  -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
43063-935-0143063093501100 TABLET in 1 BOTTLE, PLASTIC (43063-935-01)

Linked data

RxNorm, label and prices

RxNorm concepts

Related lookups

  • FDA label sections

    GET /v1/drugs/labels/f130c9c0-45d8-42bc-a040-04bb077671f8

Use it

Look up 43063-935 from code or an agent

curl
curl https://api.healthcare.dev/v1/drugs/ndc/43063-935 \
  -H "Authorization: Bearer $HDEV_API_KEY"
MCP prompt
Using the healthcare.dev MCP server, look up NDC 43063-935. 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.