Diflunisal 00093-9222
Product NDC
00093-9222- Manufacturer
- Teva Pharmaceuticals Usa, Inc.
- Dosage Form
- Tablet, Film Coated
- Route
- Oral
- Product Type
- Human Prescription Drug
- Marketing Start
- June 30, 2021
- Listing Expires
- December 31, 2026
- Application
- ANDA073673
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Active Ingredients
| Ingredient | Strength |
|---|---|
| Diflunisal | 500 mg/1 |
Drug Class
Nonsteroidal Anti-inflammatory Drug [EPC]Anti-Inflammatory AgentsNon-Steroidal [CS]
Packaging Options(3)
100 TABLET, FILM COATED in 1 BOTTLE (0093-9222-01)
500 TABLET, FILM COATED in 1 BOTTLE (0093-9222-05)
60 TABLET, FILM COATED in 1 BOTTLE (0093-9222-06)