Nabumetone
- Product NDC
- 68788-9909
- 11-digit product format
- 687889909
- Labeler code
- 68788
- Product ID
- 68788-9909_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
- 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 |
|---|
| 68788-9909-1 | 68788990901 | 100 TABLET, FILM COATED in 1 BOTTLE (68788-9909-1) | 2012-01-30 | 0000-00-00 | No | No | Current |
| 68788-9909-2 | 68788990902 | 20 TABLET, FILM COATED in 1 BOTTLE (68788-9909-2) | 2012-01-30 | 0000-00-00 | No | No | Current |
| 68788-9909-3 | 68788990903 | 30 TABLET, FILM COATED in 1 BOTTLE (68788-9909-3) | 2012-01-30 | 0000-00-00 | No | No | Current |
| 68788-9909-6 | 68788990906 | 60 TABLET, FILM COATED in 1 BOTTLE (68788-9909-6) | 2012-01-30 | 0000-00-00 | No | No | Current |
| 68788-9909-8 | 68788990908 | 120 TABLET, FILM COATED in 1 BOTTLE (68788-9909-8) | 2012-01-30 | 0000-00-00 | No | No | Current |
| 68788-9909-9 | 68788990909 | 90 TABLET, FILM COATED in 1 BOTTLE (68788-9909-9) | 2012-01-30 | 0000-00-00 | No | No | Current |