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Nabumetone

NDC 70954-784, Nabumetone, tablet, film coated, from ANI Pharmaceuticals, Inc..

Product NDC
70954-784
Status
Listed
Labeler
ANI Pharmaceuticals, Inc.
Dosage form
TABLET, FILM COATED
Route
ORAL
Product type
HUMAN PRESCRIPTION DRUG
Marketing category
ANDA
Application
ANDA219118
DEA schedule
None
Request
curl https://api.healthcare.dev/v1/drugs/ndc/70954-784 \
  -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
70954-784-1070954078410100 TABLET, FILM COATED in 1 BOTTLE (70954-784-10)
70954-784-2070954078420500 TABLET, FILM COATED in 1 BOTTLE (70954-784-20)

Linked data

RxNorm, label and prices

RxNorm concepts

Related lookups

  • FDA label sections

    GET /v1/drugs/labels/e87289f4-d4f9-4510-aaa5-51f8f8167658

  • NADAC price for package 70954078410

    GET /v1/drugs/nadac/70954078410

Use it

Look up 70954-784 from code or an agent

curl
curl https://api.healthcare.dev/v1/drugs/ndc/70954-784 \
  -H "Authorization: Bearer $HDEV_API_KEY"
MCP prompt
Using the healthcare.dev MCP server, look up NDC 70954-784. 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.