NDC 72189-667
Ibuprofen Famotidine 800 mg / 26.6 mg tablet
On the label: Direct Rx. It's repackaged: Direct Rx 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
- Direct Rx, Dawsonville, GA, United States · 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 ANDA218684
- On the market since
- Jun 22, 2026
- Package NDCs
72189-667-90- Official label
- DailyMed (National Library of Medicine), updated Jun 22, 2026
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