NDC 50268-641
Paroxetine 20 mg tablet, film coated
On the label: AvPAK. It's repackaged: AvPAK rebottles it from Aurolife Pharma LLC's NDC 13107-155.
Where the pills inside were made
| Factory | Where | Role | Last FDA inspection |
|---|---|---|---|
| Aurobindo Pharma Limited | Medchal, India | Makes it and tests it | Problems found, fixed voluntarilyJul 21, 2023 · 13 inspections, 1 with FDA action |
| Aurolife Pharma LLC | Dayton, NJ, United States | Makes it | Serious problems, FDA actionDec 7, 2021 · 10 inspections, 1 with FDA action |
Product details
- Generic drug
- Paroxetine: every company that makes it
- Form
- tablet, film coated
- Strength
- 20 mg
- Approval
- ANDA ANDA078406
- On the market since
- Mar 11, 2016
- Package NDCs
50268-641-1150268-641-15- Official label
- DailyMed (National Library of Medicine), updated Mar 24, 2026
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