Nabumetone 72189-0072
Product NDC
72189-0072- Manufacturer
- Direct Rx
- Dosage Form
- Tablet
- Route
- Oral
- Product Type
- Human Prescription Drug
- Marketing Start
- June 18, 2020
- Listing Expires
- December 31, 2026
- Application
- ANDA078420
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Active Ingredients
| Ingredient | Strength |
|---|---|
| Nabumetone | 750 mg/1 |
Drug Class
Nonsteroidal Anti-inflammatory Drug [EPC]Anti-Inflammatory AgentsNon-Steroidal [CS]
Packaging Options(3)
14 TABLET in 1 BOTTLE (72189-072-14)
30 TABLET in 1 BOTTLE (72189-072-30)
60 TABLET in 1 BOTTLE (72189-072-60)