Etodolac 00093-1118
Product NDC
00093-1118- Manufacturer
- Teva Pharmaceuticals Usa, Inc.
- Dosage Form
- Tablet, Film Coated, Extended Release
- Route
- Oral
- Product Type
- Human Prescription Drug
- Marketing Start
- August 17, 2000
- Listing Expires
- December 31, 2026
- Application
- ANDA075665
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Active Ingredients
| Ingredient | Strength |
|---|---|
| Etodolac | 600 mg/1 |
Drug Class
Nonsteroidal Anti-inflammatory Drug [EPC]Anti-Inflammatory AgentsNon-Steroidal [CS]
Packaging Options(1)
100 TABLET, FILM COATED, EXTENDED RELEASE in 1 BOTTLE (0093-1118-01)