United States · FDA National Drug Code directory
Etodolac
A source-listed medicine record.
Factual source checks only. This page is not a clinically reviewed monograph. Historical or discontinued records may be included; listing does not confirm approval, current availability or pharmacy stock.
Medicine identity
- Source reference
- 65841-777_12ad7193-e8e8-49cd-871c-e7a4c47f32c4
- Product NDC
- 65841-777
- Form
- TABLET, FILM COATED, EXTENDED RELEASE
- Composition / generic term
- Etodolac
- Labeler
- Zydus Lifesciences Limited
- Marketing category
- ANDA
- Marketing start / end (source format)
- 20140215
- Source listing expiry
- 20261231
Source-listed ingredients
- ETODOLAC — 400 mg/1
These values do not establish equivalence or a dose recommendation.
Packages
- 100 TABLET, FILM COATED, EXTENDED RELEASE in 1 BOTTLE (65841-777-01) · 65841-777-01
- 500 TABLET, FILM COATED, EXTENDED RELEASE in 1 BOTTLE (65841-777-05) · 65841-777-05
- 1000 TABLET, FILM COATED, EXTENDED RELEASE in 1 BOTTLE (65841-777-10) · 65841-777-10
- 60 TABLET, FILM COATED, EXTENDED RELEASE in 1 BOTTLE (65841-777-14) · 65841-777-14
- 100 BLISTER PACK in 1 CARTON (65841-777-77) / 1 TABLET, FILM COATED, EXTENDED RELEASE in 1 BLISTER PACK (65841-777-30) · 65841-777-77
Source and coverage
Open FDA National Drug Code directory →
Snapshot retrieved: 2026-09-17. This is the acquisition date, not a medical review date.
Clinical information, images and comparisons appear only when separately reviewed for this record. Coverage may be incomplete. Ask a pharmacist or clinician about your treatment.
Browse United States records →