NDC 51662-1564
Ziprasidone Mesylate 20 mg per 1 mL injection, powder, lyophilized, for solution
On the label: HF Acquisition Co. LLC. DBA HealthFirst. It's repackaged: HF Acquisition Co. LLC. DBA HealthFirst rebottles it from Dr. Reddy's Laboratories Inc.'s NDC 43598-848.
Where the pills inside were made
| Factory | Where | Role | Last FDA inspection |
|---|---|---|---|
| Gland Pharma Limited | Hyderabad, India | Makes it and tests it | Problems found, fixed voluntarilyJun 27, 2023 · 4 inspections |
Repackaging site
- HF Acquisition Co LLC, Mukilteo, WA, United States · relabels it
Product details
- Generic drug
- Ziprasidone: every company that makes it
- Form
- injection, powder, lyophilized, for solution, intramuscular
- Strength
- 20 mg per 1 mL
- Approval
- ANDA ANDA211908
- On the market since
- Jul 17, 2021
- Package NDCs
51662-1564-251662-1564-3- Official label
- DailyMed (National Library of Medicine), updated Jan 30, 2024
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