NDC 67046-2031
Ziprasidone Hydrochloride 20 mg capsule
On the label: Coupler LLC. It's repackaged: Coupler LLC rebottles it from BluePoint Laboratories.'s NDC 68001-450.
Where the pills inside were made
| Factory | Where | Role | Last FDA inspection |
|---|---|---|---|
| Aurobindo Pharma Limited | Mahabubnagar, India | Makes it and tests it | Problems found, fixed voluntarilyMay 10, 2022 · 7 inspections, 1 with FDA action |
Repackaging site
- Coupler LLC, West Chester, PA, United States · repackages it
Product details
- Generic drug
- Ziprasidone: every company that makes it
- Form
- capsule
- Strength
- 20 mg
- Approval
- ANDA ANDA204117
- On the market since
- Nov 8, 2024
- Package NDCs
67046-2031-3- Official label
- DailyMed (National Library of Medicine), updated Nov 8, 2024
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