NDC 60687-845
Fluoxetine 20 mg per 5 mL solution
On the label: American Health Packaging. It's repackaged: American Health Packaging rebottles it from Aurobindo Pharma Limited's NDC 65862-306.
Where the pills inside were made
| Factory | Where | Role | Last FDA inspection |
|---|---|---|---|
| Aurobindo Pharma Limited | Medchal, India | Makes it and tests it | Problems found, fixed voluntarilyJul 21, 2023 · 13 inspections, 1 with FDA action |
Repackaging site
- American Health Packaging, Columbus, OH, United States · tests it and repackages it
Product details
- Generic drug
- Fluoxetine: every company that makes it
- Form
- solution, oral
- Strength
- 20 mg per 5 mL
- Approval
- ANDA ANDA079209
- On the market since
- Dec 4, 2024
- Package NDCs
60687-845-4060687-845-4660687-845-77- Official label
- DailyMed (National Library of Medicine), updated Apr 4, 2025
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