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Nabumetone

NDC 70518-3835, Nabumetone, tablet, from REMEDYREPACK INC..

Product NDC
70518-3835
Status
Listed
Labeler
REMEDYREPACK INC.
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/70518-3835 \
  -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
70518-3835-07051838350014 TABLET in 1 BOTTLE, PLASTIC (70518-3835-0)
70518-3835-17051838350160 TABLET in 1 BOTTLE, PLASTIC (70518-3835-1)

Linked data

RxNorm, label and prices

RxNorm concepts

Related lookups

  • FDA label sections

    GET /v1/drugs/labels/311ae656-55d2-4116-a1bd-6f4a4ce70185

Use it

Look up 70518-3835 from code or an agent

curl
curl https://api.healthcare.dev/v1/drugs/ndc/70518-3835 \
  -H "Authorization: Bearer $HDEV_API_KEY"
MCP prompt
Using the healthcare.dev MCP server, look up NDC 70518-3835. 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.