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Etodolac

NDC 51672-4036, Etodolac, tablet, film coated, from Sun Pharmaceutical Industries, Inc..

Product NDC
51672-4036
Status
Listed
Labeler
Sun Pharmaceutical Industries, Inc.
Dosage form
TABLET, FILM COATED
Route
ORAL
Product type
HUMAN PRESCRIPTION DRUG
Marketing category
ANDA
Application
ANDA075074
DEA schedule
None
Request
curl https://api.healthcare.dev/v1/drugs/ndc/51672-4036 \
  -H "Authorization: Bearer $HDEV_API_KEY"

Product

Active ingredients and packages

Active ingredients

  • ETODOLAC500 mg/1

Pharmacologic classes

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

Package NDCNDC-11Package
51672-4036-151672403601100 TABLET, FILM COATED in 1 BOTTLE (51672-4036-1)

Linked data

RxNorm, label and prices

RxNorm concepts

Related lookups

  • FDA label sections

    GET /v1/drugs/labels/ec82b108-6a6f-4d1b-82cb-831d4ed36c80

  • NADAC price for package 51672403601

    GET /v1/drugs/nadac/51672403601

Use it

Look up 51672-4036 from code or an agent

curl
curl https://api.healthcare.dev/v1/drugs/ndc/51672-4036 \
  -H "Authorization: Bearer $HDEV_API_KEY"
MCP prompt
Using the healthcare.dev MCP server, look up NDC 51672-4036. 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.