Nabumetone
- Product NDC
- 71335-0939
- 11-digit product format
- 713350939
- Labeler code
- 71335
- Product ID
- 71335-0939_20c4c4da-3e8f-49cd-b16e-c2a1b4592f91
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- Nabumentone
- Dosage form
- TABLET
- Route
- ORAL
- Labeler
- Bryant Ranch Prepack
- Application
- ANDA075280
- Marketing category
- ANDA
- Marketing start
- 2002-02-25
- Marketing end
- 0000-00-00
- Substance
- NABUMETONE
- Active strength
- 750 mg/1
- Pharmacologic classes
- Cyclooxygenase Inhibitors [MoA],Anti-Inflammatory Agents, Non-Steroidal [CS],Nonsteroidal Anti-inflammatory Drug [EPC]
- NDC exclude flag
- No
- Listing certified through
- 2021-12-31
- Current FDA listing
- Historical FDA.report record
Packages#
Package NDC, 11-digit format, Description table| Package NDC | 11-digit format | Description | Units | Marketing start | Marketing end | Sample | Exclude flag | Status |
|---|
| 71335-0939-1 | 71335093901 | 30 TABLET in 1 BOTTLE (71335-0939-1) | 30 tablet | 2007-03-29 | 0000-00-00 | No | No | Current |
| 71335-0939-2 | 71335093902 | 60 TABLET in 1 BOTTLE (71335-0939-2) | 60 tablet | 2007-03-29 | 0000-00-00 | No | No | Current |
| 71335-0939-3 | 71335093903 | 90 TABLET in 1 BOTTLE (71335-0939-3) | 90 tablet | 2007-03-29 | 0000-00-00 | No | No | Current |
| 71335-0939-4 | 71335093904 | 120 TABLET in 1 BOTTLE (71335-0939-4) | 120 tablet | 2007-03-29 | 0000-00-00 | No | No | Current |
| 71335-0939-5 | 71335093905 | 180 TABLET in 1 BOTTLE (71335-0939-5) | 180 tablet | 2007-03-29 | 0000-00-00 | No | No | Current |
| 71335-0939-6 | 71335093906 | 300 TABLET in 1 BOTTLE (71335-0939-6) | 300 tablet | 2007-03-29 | 0000-00-00 | No | No | Current |
| 71335-0939-7 | 71335093907 | 500 TABLET in 1 BOTTLE (71335-0939-7) | 500 tablet | 2007-03-29 | 0000-00-00 | No | No | Current |