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Nabumetone

NDC 71205-530, Nabumetone, tablet, from Proficient Rx LP.

Product NDC
71205-530
Status
Listed
Labeler
Proficient Rx LP
Dosage form
TABLET
Route
ORAL
Product type
HUMAN PRESCRIPTION DRUG
Marketing category
ANDA
Application
ANDA078420
DEA schedule
None
Request
curl https://api.healthcare.dev/v1/drugs/ndc/71205-530 \
  -H "Authorization: Bearer $HDEV_API_KEY"

Product

Active ingredients and packages

Active ingredients

  • NABUMETONE750 mg/1

Pharmacologic classes

Anti-Inflammatory Agents, Non-Steroidal [CS]; Cyclooxygenase Inhibitors [MoA]; Nonsteroidal Anti-inflammatory Drug [EPC]

Package NDCNDC-11Package
71205-530-307120505303030 TABLET in 1 BOTTLE (71205-530-30)
71205-530-607120505306060 TABLET in 1 BOTTLE (71205-530-60)
71205-530-907120505309090 TABLET in 1 BOTTLE (71205-530-90)

Linked data

RxNorm, label and prices

RxNorm concepts

Related lookups

  • FDA label sections

    GET /v1/drugs/labels/f4392863-ed3f-4fbd-8260-49827609aa2e

Use it

Look up 71205-530 from code or an agent

curl
curl https://api.healthcare.dev/v1/drugs/ndc/71205-530 \
  -H "Authorization: Bearer $HDEV_API_KEY"
MCP prompt
Using the healthcare.dev MCP server, look up NDC 71205-530. 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.