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Nabumetone

NDC 80425-0053, Nabumetone, tablet, film coated, from Advanced Rx of Tennessee, LLC.

Product NDC
80425-0053
Status
Listed
Labeler
Advanced Rx of Tennessee, LLC
Dosage form
TABLET, FILM COATED
Route
ORAL
Product type
HUMAN PRESCRIPTION DRUG
Marketing category
ANDA
Application
ANDA078671
DEA schedule
None
Request
curl https://api.healthcare.dev/v1/drugs/ndc/80425-0053 \
  -H "Authorization: Bearer $HDEV_API_KEY"

Product

Active ingredients and packages

Active ingredients

  • NABUMETONE500 mg/1

Pharmacologic classes

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

Package NDCNDC-11Package
80425-0053-18042500530160 TABLET, FILM COATED in 1 BOTTLE (80425-0053-1)

Linked data

RxNorm, label and prices

RxNorm concepts

Related lookups

  • FDA label sections

    GET /v1/drugs/labels/af9969df-ce14-c0bc-e053-2995a90a3f59

Use it

Look up 80425-0053 from code or an agent

curl
curl https://api.healthcare.dev/v1/drugs/ndc/80425-0053 \
  -H "Authorization: Bearer $HDEV_API_KEY"
MCP prompt
Using the healthcare.dev MCP server, look up NDC 80425-0053. 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.