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Allopurinol

NDC 71205-377, Allopurinol, tablet, from Proficient Rx LP.

Product NDC
71205-377
Status
Listed
Labeler
Proficient Rx LP
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/71205-377 \
  -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
71205-377-307120503773030 TABLET in 1 BOTTLE, PLASTIC (71205-377-30)
71205-377-607120503776060 TABLET in 1 BOTTLE, PLASTIC (71205-377-60)
71205-377-907120503779090 TABLET in 1 BOTTLE, PLASTIC (71205-377-90)

Linked data

RxNorm, label and prices

RxNorm concepts

Related lookups

  • FDA label sections

    GET /v1/drugs/labels/b20c6ed4-6b94-4a1b-b448-e910856fa825

Use it

Look up 71205-377 from code or an agent

curl
curl https://api.healthcare.dev/v1/drugs/ndc/71205-377 \
  -H "Authorization: Bearer $HDEV_API_KEY"
MCP prompt
Using the healthcare.dev MCP server, look up NDC 71205-377. 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.