Nabumetone
- Product NDC
- 71205-978
- 11-digit product format
- 712050978
- Labeler code
- 71205
- Product ID
- 71205-978_40ce485f-575c-4c51-8058-83b10a8ddac7
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- Nabumetone
- Dosage form
- TABLET
- Route
- ORAL
- Labeler
- Proficient Rx LP
- Application
- ANDA078420
- Marketing category
- ANDA
- Marketing start
- 2019-09-25
- 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 |
|---|
| 71205-978-00 | 71205097800 | 100 TABLET in 1 BOTTLE, PLASTIC (71205-978-00) | 100 tablet | 2020-05-07 | No | No | Historical |
| 71205-978-30 | 71205097830 | 30 TABLET in 1 BOTTLE, PLASTIC (71205-978-30) | 30 tablet | 2020-05-07 | No | No | Historical |
| 71205-978-55 | 71205097855 | 500 TABLET in 1 BOTTLE, PLASTIC (71205-978-55) | 500 tablet | 2020-05-07 | No | No | Historical |
| 71205-978-60 | 71205097860 | 60 TABLET in 1 BOTTLE, PLASTIC (71205-978-60) | 60 tablet | 2020-05-07 | No | No | Historical |
| 71205-978-72 | 71205097872 | 120 TABLET in 1 BOTTLE, PLASTIC (71205-978-72) | 120 tablet | 2020-05-07 | No | No | Historical |
| 71205-978-90 | 71205097890 | 90 TABLET in 1 BOTTLE, PLASTIC (71205-978-90) | 90 tablet | 2020-05-07 | No | No | Historical |
Related DailyMed Labels
| Title | Manufacturer | Effective date | Type | Version |
|---|
| NABUMETONE TABLETS USP | Proficient Rx LP | 2022-05-01 | HUMAN PRESCRIPTION DRUG LABEL | 3 |