NDC 85509-1495
Naproxen sodium 550 mg tablet, film coated
On the label: Phoenix RX LLC. It's repackaged: Phoenix RX LLC rebottles it from Dr. Reddy's Laboratories Inc.'s NDC 43598-495.
Where the pills inside were made
| Factory | Where | Role | Last FDA inspection |
|---|---|---|---|
| Dr. Reddy's Laboratories Limited | Medchal-Malkajgiri, India | Makes it and tests it | Problems found, fixed voluntarilyOct 27, 2023 · 8 inspections |
Repackaging site
- Phoenix RX LLC, Hatboro, PA, United States · repackages it and relabels it
Product details
- Generic drug
- Naproxen: every company that makes it
- Form
- tablet, film coated, oral
- Strength
- 550 mg
- Approval
- ANDA ANDA078486
- On the market since
- Apr 26, 2016
- Package NDCs
85509-1495-385509-1495-685509-1495-9- Official label
- DailyMed (National Library of Medicine), updated Feb 24, 2026
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