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Etodolac

NDC 0093-7172, Etodolac, tablet, film coated, extended release, from Teva Pharmaceuticals USA, Inc..

Product NDC
0093-7172
Status
Listed
Labeler
Teva Pharmaceuticals USA, Inc.
Dosage form
TABLET, FILM COATED, EXTENDED RELEASE
Route
ORAL
Product type
HUMAN PRESCRIPTION DRUG
Marketing category
ANDA
Application
ANDA075665
DEA schedule
None
Request
curl https://api.healthcare.dev/v1/drugs/ndc/0093-7172 \
  -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
0093-7172-0100093717201100 TABLET, FILM COATED, EXTENDED RELEASE in 1 BOTTLE (0093-7172-01)

Linked data

RxNorm, label and prices

RxNorm concepts

Related lookups

  • FDA label sections

    GET /v1/drugs/labels/f3bf1675-8fda-40d3-8427-0a6a6133a3d3

  • NADAC price for package 00093717201

    GET /v1/drugs/nadac/00093717201

Use it

Look up 0093-7172 from code or an agent

curl
curl https://api.healthcare.dev/v1/drugs/ndc/0093-7172 \
  -H "Authorization: Bearer $HDEV_API_KEY"
MCP prompt
Using the healthcare.dev MCP server, look up NDC 0093-7172. 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.