Nabumetone
- Product NDC
- 71335-2292
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- Nabumetone
- Dosage form
- TABLET
- Route
- ORAL
- Labeler
- Bryant Ranch Prepack
- Application
- ANDA078420
- Marketing category
- ANDA
- Substance
- NABUMETONE
- Current FDA listing
- Yes
Related Records
Packages
| Package NDC | Description | Marketing start | Marketing end | Sample | Status |
|---|---|---|---|---|---|
| 71335-2292-1 | 500 TABLET in 1 BOTTLE (71335-2292-1) | 2023-12-01 | No | Historical |
Related DailyMed Labels
| Title | Manufacturer | Effective date | Type | Version |
|---|---|---|---|---|
| NABUMETONE TABLETS USP Rx Only | Bryant Ranch Prepack | 2025-03-31 | HUMAN PRESCRIPTION DRUG LABEL | 101 |