NDC 51655-274
Fluoxetine 20 mg capsule
On the label: Northwind Pharmaceuticals. It's repackaged: Northwind Pharmaceuticals rebottles it from ScieGen Pharmaceuticals, Inc.'s NDC 50228-114.
Where the pills inside were made
| Factory | Where | Role | Last FDA inspection |
|---|---|---|---|
| ScieGen Pharmaceuticals, INC. | Hauppauge, NY, United States | Makes it and tests it | Problems found, fixed voluntarilyMay 15, 2026 · 15 inspections, 1 with FDA action |
Repackaging site
- Northwind Health Company, LLC, Indianapolis, IN, United States · repackages it
Product details
- Generic drug
- Fluoxetine: every company that makes it
- Form
- capsule, oral
- Strength
- 20 mg
- Approval
- ANDA ANDA204597
- On the market since
- May 20, 2020
- Package NDCs
51655-274-26- Official label
- DailyMed (National Library of Medicine), updated Jan 1, 2026
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