NDC 42708-182
Fluoxetine 20 mg capsule
On the label: QPharma, Inc.. It's repackaged: QPharma, Inc. 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 |
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 ANDA078619
- On the market since
- Jan 31, 2008
- Package NDCs
42708-182-30- Official label
- DailyMed (National Library of Medicine), updated Dec 2, 2025
Got it by mail or from a pharmacy you don't know? Look the pharmacy up on Who Filled My Rx?