Nabumetone
- Product NDC
- 68788-9908
- 11-digit product format
- 687889908
- Labeler code
- 68788
- Product ID
- 68788-9908_b3ea0031-6eda-4893-b076-8b77e63a6e45
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- Nabumetone
- Dosage form
- TABLET, FILM COATED
- Route
- ORAL
- Labeler
- Preferred Pharmaceuticals, Inc.
- Application
- ANDA078671
- Marketing category
- ANDA
- Marketing start
- 2012-01-30
- Marketing end
- 0000-00-00
- Substance
- NABUMETONE
- Active strength
- 500 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 |
|---|
| 68788-9908-1 | 68788990801 | 100 TABLET, FILM COATED in 1 BOTTLE (68788-9908-1) | 2012-01-30 | 0000-00-00 | No | No | Current |
| 68788-9908-2 | 68788990802 | 20 TABLET, FILM COATED in 1 BOTTLE (68788-9908-2) | 2012-01-30 | 0000-00-00 | No | No | Current |
| 68788-9908-3 | 68788990803 | 30 TABLET, FILM COATED in 1 BOTTLE (68788-9908-3) | 2012-01-30 | 0000-00-00 | No | No | Current |
| 68788-9908-6 | 68788990806 | 60 TABLET, FILM COATED in 1 BOTTLE (68788-9908-6) | 2012-01-30 | 0000-00-00 | No | No | Current |
| 68788-9908-8 | 68788990808 | 120 TABLET, FILM COATED in 1 BOTTLE (68788-9908-8) | 2012-01-30 | 0000-00-00 | No | No | Current |
| 68788-9908-9 | 68788990809 | 90 TABLET, FILM COATED in 1 BOTTLE (68788-9908-9) | 2012-01-30 | 0000-00-00 | No | No | Current |