NDC 62175-472
Paroxetine Hydrochloride 37.5 mg tablet, film coated, extended release
On the label: Lannett Company, Inc..
Where it's made
| Factory | Where | Role | Last FDA inspection |
|---|---|---|---|
| Lannett Company, LLC | Seymour, IN, United States | Makes it | Problems found, fixed voluntarilyOct 21, 2022 · 9 inspections, 1 with FDA action |
Product details
- Generic drug
- Paroxetine: every company that makes it
- Form
- tablet, film coated, extended release, oral
- Strength
- 37.5 mg
- Approval
- ANDA ANDA204744
- On the market since
- Oct 31, 2014
- Package NDCs
62175-472-3262175-472-41- Official label
- DailyMed (National Library of Medicine), updated Oct 8, 2026
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