Nabumetone
- Product NDC
- 68788-7532
- 11-digit product format
- 687887532
- Labeler code
- 68788
- Product ID
- 68788-7532_c9c58d47-b834-4f41-a38e-e7e98b46feec
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- Nabumetone
- Dosage form
- TABLET, FILM COATED
- Route
- ORAL
- Labeler
- Preferred Pharmaceuticals, Inc.
- Application
- ANDA075189
- Marketing category
- ANDA
- Marketing start
- 2001-09-26
- 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 | Marketing start | Marketing end | Sample | Exclude flag | Status |
|---|
| 68788-7532-1 | 68788753201 | 100 TABLET, FILM COATED in 1 BOTTLE (68788-7532-1) | 2019-10-04 | 0000-00-00 | No | No | Current |
| 68788-7532-2 | 68788753202 | 20 TABLET, FILM COATED in 1 BOTTLE (68788-7532-2) | 2019-10-04 | 0000-00-00 | No | No | Current |
| 68788-7532-3 | 68788753203 | 30 TABLET, FILM COATED in 1 BOTTLE (68788-7532-3) | 2019-10-04 | 0000-00-00 | No | No | Current |
| 68788-7532-6 | 68788753206 | 60 TABLET, FILM COATED in 1 BOTTLE (68788-7532-6) | 2019-10-04 | 0000-00-00 | No | No | Current |
| 68788-7532-8 | 68788753208 | 120 TABLET, FILM COATED in 1 BOTTLE (68788-7532-8) | 2019-10-04 | 0000-00-00 | No | No | Current |
| 68788-7532-9 | 68788753209 | 90 TABLET, FILM COATED in 1 BOTTLE (68788-7532-9) | 2019-10-04 | 0000-00-00 | No | No | Current |