NDC 85534-0080
Amoxicillin and Clavulanate Potassium 200 mg per 5 mL / 28.5 mg per 5 mL powder, for suspension
On the label: Hawaii Repack, Inc.. It's repackaged: Hawaii Repack, Inc. rebottles it from Aurobindo Pharma Limited's NDC 65862-533.
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 and Clavulanic Acid: every company that makes it
- Form
- powder, for suspension, oral
- Strength
- 200 mg per 5 mL / 28.5 mg per 5 mL
- Approval
- ANDA ANDA201090
- On the market since
- Dec 20, 2011
- Package NDCs
85534-0080-085534-0080-185534-0080-2- Official label
- DailyMed (National Library of Medicine), updated Jul 13, 2026
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