NDC 33261-766
Amoxicillin 200 mg per 5 mL powder, for suspension
On the label: Aidarex Pharmaceuticals LLC. It's repackaged: Aidarex Pharmaceuticals LLC rebottles it from Aurobindo Pharma Limited's NDC 65862-070.
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
- powder, for suspension
- Strength
- 200 mg per 5 mL
- Approval
- ANDA ANDA065334
- On the market since
- Dec 28, 2006
- Package NDCs
33261-766-01- Official label
- DailyMed (National Library of Medicine), updated Nov 21, 2013
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