NDC 70518-2191
Amoxicillin 875 mg tablet, film coated
On the label: Remedyrepack Inc.. It's repackaged: Remedyrepack Inc. rebottles it from Aurobindo Pharma Limited's NDC 65862-015.
Where the pills inside were made
| Factory | Where | Role | Last FDA inspection |
|---|---|---|---|
| Aurobindo Pharma Limited | Medchal, India | Makes it and tests it | Serious problems, FDA actionSep 5, 2025 · 8 inspections, 1 with FDA action |
Product details
- Generic drug
- Amoxicillin: every company that makes it
- Form
- tablet, film coated, oral
- Strength
- 875 mg
- Approval
- ANDA ANDA065256
- On the market since
- Jul 9, 2019
- Package NDCs
70518-2191-070518-2191-170518-2191-270518-2191-370518-2191-4- Official label
- DailyMed (National Library of Medicine), updated Jul 21, 2026
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