NDC 70518-3483
Fluoxetine 10 mg capsule
On the label: Remedyrepack Inc.. It's repackaged: Remedyrepack Inc. rebottles it from ScieGen Pharmaceuticals, Inc.'s NDC 50228-113.
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 |
Product details
- Generic drug
- Fluoxetine: every company that makes it
- Form
- capsule, oral
- Strength
- 10 mg
- Approval
- ANDA ANDA204597
- On the market since
- Aug 17, 2022
- Package NDCs
70518-3483-070518-3483-1- Official label
- DailyMed (National Library of Medicine), updated Oct 13, 2026
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