Nabumetone
- Product NDC
- 63629-8510
- 11-digit product format
- 636298510
- Labeler code
- 63629
- Product ID
- 63629-8510_5f580130-9b4a-4c37-80b1-734baabb529b
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- Nabumetone
- Dosage form
- TABLET
- Route
- ORAL
- Labeler
- Bryant Ranch Prepack
- Application
- ANDA078420
- Marketing category
- ANDA
- Marketing start
- 2019-06-26
- Substance
- NABUMETONE
- Active strength
- 750 mg/1
- Pharmacologic classes
- Anti-Inflammatory Agents, Non-Steroidal [CS], Cyclooxygenase Inhibitors [MoA], Nonsteroidal Anti-inflammatory Drug [EPC]
- NDC exclude flag
- No
- Listing certified through
- 2026-12-31
- Current FDA listing
- Yes
Related UNII Ingredients
| UNII | Preferred term | Registry number | Matched term |
|---|
| LW0TIW155Z | NABUMETONE | 42924-53-8 | NABUMETONE |
Packages
| Package NDC | 11-digit format | Description | Units | Marketing start | Sample | Exclude flag | Status |
|---|
| 63629-8510-1 | 63629851001 | 100 TABLET in 1 BOTTLE (63629-8510-1) | 100 tablet | 2019-06-26 | No | No | Historical |