NDC 67046-214
Fluoxetine 20 mg capsule
On the label: Coupler Enterprises Inc.. It's repackaged: Coupler Enterprises Inc. rebottles it from Camber Pharmaceuticals Inc.'s NDC 31722-904.
Where the pills inside were made
| Factory | Where | Role | Last FDA inspection |
|---|---|---|---|
| ScieGen Pharmaceuticals, INC. | Hauppauge, NY, United States | Makes it, tests it and packages it | Problems found, fixed voluntarilyMay 15, 2026 · 15 inspections, 1 with FDA action |
Repackaging site
- Coupler Enterprises, Location not on file · repackages it
Product details
- Generic drug
- Fluoxetine: every company that makes it
- Form
- capsule
- Strength
- 20 mg
- Approval
- ANDA ANDA204597
- On the market since
- Jul 30, 2015
- Package NDCs
67046-214-3067046-214-60- Official label
- DailyMed (National Library of Medicine), updated Sep 14, 2017
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