NDC 85509-1315
Ibuprofen And Famotidine 800 mg / 26.6 mg tablet
On the label: Phoenix RX LLC. It's repackaged: Phoenix RX LLC rebottles it from Camber Pharmaceuticals Inc.'s NDC 31722-315.
Where the pills inside were made
| Factory | Where | Role | Last FDA inspection |
|---|---|---|---|
| Ascent Pharmaceuticals Inc | Central Islip, NY, United States | Makes it, tests it and packages it | Problems found, fixed voluntarilyAug 9, 2024 · 9 inspections |
Repackaging site
- Phoenix RX LLC, Hatboro, PA, United States · repackages it and relabels it
Product details
- Generic drug
- Famotidine and Ibuprofen: every company that makes it
- Form
- tablet, oral
- Strength
- 800 mg / 26.6 mg
- Approval
- ANDA ANDA216814
- On the market since
- Mar 15, 2023
- Package NDCs
85509-1315-385509-1315-685509-1315-9- Official label
- DailyMed (National Library of Medicine), updated Oct 15, 2025
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