Naproxen
- Product NDC
- 68788-7072
- 11-digit product format
- 687887072
- Labeler code
- 68788
- Product ID
- 68788-7072_6ee95eac-46fb-41c5-8d9e-097cbc25d26c
- 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
- 2018-01-02
- Marketing end
- 0000-00-00
- Substance
- NAPROXEN
- Active strength
- 375 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 |
|---|
| 68788-7072-0 | 68788707200 | 100 TABLET, DELAYED RELEASE in 1 BOTTLE (68788-7072-0) | 2018-01-02 | 0000-00-00 | No | No | Current |
| 68788-7072-2 | 68788707202 | 20 TABLET, DELAYED RELEASE in 1 BOTTLE (68788-7072-2) | 2018-01-02 | 0000-00-00 | No | No | Current |
| 68788-7072-3 | 68788707203 | 30 TABLET, DELAYED RELEASE in 1 BOTTLE (68788-7072-3) | 2018-01-02 | 0000-00-00 | No | No | Current |
| 68788-7072-4 | 68788707204 | 14 TABLET, DELAYED RELEASE in 1 BOTTLE (68788-7072-4) | 2019-11-01 | 0000-00-00 | No | No | Current |
| 68788-7072-6 | 68788707206 | 60 TABLET, DELAYED RELEASE in 1 BOTTLE (68788-7072-6) | 2018-01-02 | 0000-00-00 | No | No | Current |
| 68788-7072-9 | 68788707209 | 90 TABLET, DELAYED RELEASE in 1 BOTTLE (68788-7072-9) | 2018-01-02 | 0000-00-00 | No | No | Current |