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Nabumetone 500 mg

NDC 79739-7076, Nabumetone, tablet, film coated, from LGM PHARMA SOLUTIONS, LLC.

Product NDC
79739-7076
Status
Listed
Labeler
LGM PHARMA SOLUTIONS, LLC
Dosage form
TABLET, FILM COATED
Route
ORAL
Product type
HUMAN PRESCRIPTION DRUG
Marketing category
ANDA
Application
ANDA203166
DEA schedule
None
Request
curl https://api.healthcare.dev/v1/drugs/ndc/79739-7076 \
  -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
79739-7076-179739707601100 TABLET, FILM COATED in 1 BOTTLE (79739-7076-1)
79739-7076-579739707605500 TABLET, FILM COATED in 1 BOTTLE (79739-7076-5)

Linked data

RxNorm, label and prices

RxNorm concepts

Related lookups

  • FDA label sections

    GET /v1/drugs/labels/ef7c3da8-797f-4ea9-8999-53509785a0f7

Use it

Look up 79739-7076 from code or an agent

curl
curl https://api.healthcare.dev/v1/drugs/ndc/79739-7076 \
  -H "Authorization: Bearer $HDEV_API_KEY"
MCP prompt
Using the healthcare.dev MCP server, look up NDC 79739-7076. 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.