NDC 59651-908
Ibuprofen and famotidine 800 mg / 26.6 mg tablet, film coated
On the label: Aurobindo Pharma Limited.
Where it's made
| Factory | Where | Role | Last FDA inspection |
|---|---|---|---|
| Aurobindo Pharma Limited | Mahabubnagar, India | Makes it and tests it | Problems found, fixed voluntarilyMay 10, 2022 · 7 inspections, 1 with FDA action |
Product details
- Generic drug
- Famotidine and Ibuprofen: every company that makes it
- Form
- tablet, film coated, oral
- Strength
- 800 mg / 26.6 mg
- Approval
- ANDA ANDA219538
- On the market since
- Jun 30, 2025
- Package NDCs
59651-908-90- Official label
- DailyMed (National Library of Medicine), updated Jul 3, 2025
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