Naproxen
- Product NDC
- 68788-6908
- 11-digit product format
- 687886908
- Labeler code
- 68788
- Product ID
- 68788-6908_a8b6e14e-443a-4429-85ae-9556bc16b568
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- Naproxen
- Dosage form
- TABLET, DELAYED RELEASE
- Route
- ORAL
- Labeler
- Preferred Pharmaceuticals Inc.
- Application
- ANDA075227
- Marketing category
- ANDA
- Marketing start
- 2017-02-22
- Marketing end
- 0000-00-00
- Substance
- NAPROXEN
- 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 |
|---|
| 68788-6908-1 | 68788690801 | 100 TABLET, DELAYED RELEASE in 1 BOTTLE (68788-6908-1) | 2017-02-22 | 0000-00-00 | No | No | Current |
| 68788-6908-2 | 68788690802 | 20 TABLET, DELAYED RELEASE in 1 BOTTLE (68788-6908-2) | 2017-02-22 | 0000-00-00 | No | No | Current |
| 68788-6908-3 | 68788690803 | 30 TABLET, DELAYED RELEASE in 1 BOTTLE (68788-6908-3) | 2017-02-22 | 0000-00-00 | No | No | Current |
| 68788-6908-6 | 68788690806 | 60 TABLET, DELAYED RELEASE in 1 BOTTLE (68788-6908-6) | 2017-02-22 | 0000-00-00 | No | No | Current |
| 68788-6908-9 | 68788690809 | 90 TABLET, DELAYED RELEASE in 1 BOTTLE (68788-6908-9) | 2017-02-22 | 0000-00-00 | No | No | Current |