NDC 53808-0986
Fluoxetine Hydrochloride 20 mg tablet
On the label: State of Florida DOH Central Pharmacy. It's repackaged: State of Florida DOH Central Pharmacy rebottles it from Aurobindo Pharma Limited's NDC 65862-193.
Where the pills inside were made
| Factory | Where | Role | Last FDA inspection |
|---|---|---|---|
| Apl Healthcare Limited | Tirupati, India | Makes it and tests it | Problems found, fixed voluntarilyDec 17, 2025 · 5 inspections |
| Aurobindo Pharma Limited | Medchal, India | Makes it and tests it | Problems found, fixed voluntarilyJul 21, 2023 · 13 inspections, 1 with FDA action |
| Aurobindo Pharma Limited | Mahabubnagar, India | Makes it and tests it | Problems found, fixed voluntarilyMay 10, 2022 · 7 inspections, 1 with FDA action |
Product details
- Generic drug
- Fluoxetine: every company that makes it
- Form
- tablet
- Strength
- 20 mg
- Approval
- ANDA ANDA075049
- On the market since
- Jul 1, 2009
- Package NDCs
53808-0986-1- Official label
- DailyMed (National Library of Medicine), updated Jun 1, 2010
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