Naproxen
- Product NDC
- 50090-3036
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- Naproxen
- Dosage form
- TABLET
- Route
- ORAL
- Labeler
- A-S Medication Solutions
- Application
- ANDA075927
- Marketing category
- ANDA
- Substance
- NAPROXEN
- Current FDA listing
- Historical FDA.report record
Packages
| Package NDC | Description | Marketing start | Marketing end | Sample | Status |
|---|
| 50090-3036-0 | 15 TABLET in 1 BOTTLE (50090-3036-0) | 2017-06-07 | 0000-00-00 | No | Current |
| 50090-3036-1 | 20 TABLET in 1 BOTTLE, PLASTIC (50090-3036-1) | 2014-11-28 | 0000-00-00 | No | Current |
| 50090-3036-2 | 30 TABLET in 1 BOTTLE, PLASTIC (50090-3036-2) | 2014-11-28 | 0000-00-00 | No | Current |
| 50090-3036-4 | 14 TABLET in 1 BOTTLE, PLASTIC (50090-3036-4) | 2014-11-28 | 0000-00-00 | No | Current |
| 50090-3036-5 | 40 TABLET in 1 BOTTLE, PLASTIC (50090-3036-5) | 2014-11-28 | 0000-00-00 | No | Current |
| 50090-3036-6 | 100 TABLET in 1 BOTTLE (50090-3036-6) | 2019-10-21 | 0000-00-00 | No | Current |
| 50090-3036-7 | 60 TABLET in 1 BOTTLE, PLASTIC (50090-3036-7) | 2014-11-28 | 0000-00-00 | No | Current |
| 50090-3036-9 | 6 TABLET in 1 BOTTLE (50090-3036-9) | 2019-10-21 | 0000-00-00 | No | Current |