NDC 70518-2182
Paroxetine 30 mg tablet, film coated
On the label: Remedyrepack Inc.. It's repackaged: Remedyrepack Inc. rebottles it from Solco Healthcare U.S., LLC's NDC 43547-349.
Where the pills inside were made
| Factory | Where | Role | Last FDA inspection |
|---|---|---|---|
| Zhejiang Huahai Pharmaceutical Co., Ltd. | Linhai, China | Makes it | Serious problems, FDA actionApr 24, 2026 · 8 inspections, 3 with FDA action |
| Zhejiang Huahai Pharmaceutical Technology Co., Ltd. | Taizhou, China | Makes it | Problems found, fixed voluntarilyAug 22, 2025 · 1 inspection |
Product details
- Generic drug
- Paroxetine: every company that makes it
- Form
- tablet, film coated, oral
- Strength
- 30 mg
- Approval
- ANDA ANDA203854
- On the market since
- Jul 1, 2019
- Package NDCs
70518-2182-070518-2182-170518-2182-2- Official label
- DailyMed (National Library of Medicine), updated Jul 29, 2026
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