NDC 76420-718
Paroxetine 30 mg tablet, film coated
On the label: Asclemed USA, Inc.. It's repackaged: Asclemed USA, Inc. rebottles it from Zydus Pharmaceuticals (USA) Inc.'s NDC 68382-099.
Where the pills inside were made
| Factory | Where | Role | Last FDA inspection |
|---|---|---|---|
| Zydus Lifesciences Limited | Ahmedabad, India | Makes it and tests it | Problems found, fixed voluntarilyAug 5, 2022 · 10 inspections, 3 with FDA action |
| Zydus Lifesciences Limited | Solan, India | Makes it and tests it | No problems foundMar 9, 2020 · 6 inspections |
Repackaging site
- Asclemed USA Inc. dba Enovachem, Torrance, CA, United States · repackages it and relabels it
Recalls
- Nov 20, 2017 · Class II · Zydus Pharmaceuticals USA Inc
Presence of Foreign Tablets/Capsules: Risperidone Tablets were found in bottle of Paroxetine Tablets
Lots: a) Z701308, b) Z701309, c) Z701310 exp April 2019 - Aug 18, 2017 · Class II · Zydus Pharmaceuticals USA Inc
Presence of Foreign tablets/capsules: risperidone Tablets were found in bottle of paroxetine Tablets
Lots: Lot #: Z701133, Exp 03/19
Class I recalls are the most serious; Class III the least. A recall covers specific lots, listed on each recall.
Product details
- Generic drug
- Paroxetine: every company that makes it
- Form
- tablet, film coated, oral
- Strength
- 30 mg
- Approval
- ANDA ANDA077584
- On the market since
- Apr 13, 2007
- Package NDCs
76420-718-0176420-718-0576420-718-1076420-718-3076420-718-6076420-718-90- Official label
- DailyMed (National Library of Medicine), updated Feb 13, 2025
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