Naproxen
- Product NDC
- 71335-0318
- 11-digit product format
- 713350318
- Labeler code
- 71335
- Product ID
- 71335-0318_826055a0-ecd5-45cb-bb08-c3506d65a391
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- Naproxen
- Dosage form
- TABLET, DELAYED RELEASE
- Route
- ORAL
- Labeler
- Bryant Ranch Prepack
- Application
- ANDA091432
- Marketing category
- ANDA
- Marketing start
- 2016-07-05
- 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 |
|---|
| 71335-0318-1 | 71335031801 | 42 TABLET, DELAYED RELEASE in 1 BOTTLE (71335-0318-1) | 2016-07-05 | 0000-00-00 | No | No | Current |
| 71335-0318-2 | 71335031802 | 60 TABLET, DELAYED RELEASE in 1 BOTTLE (71335-0318-2) | 2016-07-05 | 0000-00-00 | No | No | Current |
| 71335-0318-3 | 71335031803 | 30 TABLET, DELAYED RELEASE in 1 BOTTLE (71335-0318-3) | 2016-07-05 | 0000-00-00 | No | No | Current |
| 71335-0318-4 | 71335031804 | 100 TABLET, DELAYED RELEASE in 1 BOTTLE (71335-0318-4) | 2016-07-05 | 0000-00-00 | No | No | Current |
| 71335-0318-5 | 71335031805 | 15 TABLET, DELAYED RELEASE in 1 BOTTLE (71335-0318-5) | 2016-07-05 | 0000-00-00 | No | No | Current |
| 71335-0318-6 | 71335031806 | 120 TABLET, DELAYED RELEASE in 1 BOTTLE (71335-0318-6) | 2016-07-05 | 0000-00-00 | No | No | Current |
| 71335-0318-7 | 71335031807 | 90 TABLET, DELAYED RELEASE in 1 BOTTLE (71335-0318-7) | 2016-07-05 | 0000-00-00 | No | No | Current |
| 71335-0318-8 | 71335031808 | 14 TABLET, DELAYED RELEASE in 1 BOTTLE (71335-0318-8) | 2016-07-05 | 0000-00-00 | No | No | Current |