Composition
- Active ingredients
- ETODOLAC 400MG **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons**
Strengths and forms
The FDA lists each strength of a product separately; these pages share one label.
- ETODOLAC 500MG **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons** · Tablet, extended releaseNDA020584-003 · Discontinued
- ETODOLAC 400MG **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons** · Tablet, extended releaseThis page
- ETODOLAC 600MG **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons** · Tablet, extended releaseNDA020584-002 · Discontinued
Official product information
Drugs@FDA lists the approved labels, letters and reviews for application NDA020584.
Prognia shows this product information for reference and learning. It is not treatment advice and can lag behind the official text. Always check the current product information and local protocols before prescribing.
At a glance
- Brand name
- Lodine XL
- Active substance
- etodolac
- Route
- Oral
- Dosage form
- Tablet, extended release
- Applicant
- Wyeth Pharms Inc
- Status
- Discontinued
- FDA approval
- 25 Oct 1996
- Application
- NDA020584-001