NDC 80425-0587
Ibuprofen and Famotidine 800 mg / 26.6 mg tablet
On the label: Advanced Rx Pharmacy of Tennessee, LLC. It's repackaged: Advanced Rx Pharmacy of Tennessee, LLC rebottles it from Viona Pharmaceuticals Inc.'s NDC 72578-214.
Where the pills inside were made
| Factory | Where | Role | Last FDA inspection |
|---|---|---|---|
| Zydus Lifesciences Limited | Ahmedabad, India | Makes it and tests it | Problems found, fixed voluntarilyMar 24, 2023 · 5 inspections |
Repackaging site
- Advanced Rx Pharmacy of Tennessee, LLC, Nashville, TN, United States · repackages it
Product details
- Generic drug
- Famotidine and Ibuprofen: every company that makes it
- Form
- tablet, oral
- Strength
- 800 mg / 26.6 mg
- Approval
- ANDA ANDA218684
- On the market since
- Jun 18, 2026
- Package NDCs
80425-0587-180425-0587-280425-0587-3- Official label
- DailyMed (National Library of Medicine), updated Jun 18, 2026
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