NDC 51662-1623
Vasopressin 20 [USP'U] per 1 mL injection
On the label: HF Acquisition Co. LLC. DBA HealthFirst. It's repackaged: HF Acquisition Co. LLC. DBA HealthFirst rebottles it from AuroMedics Pharma LLC's NDC 55150-370.
Where the pills inside were made
| Factory | Where | Role | Last FDA inspection |
|---|---|---|---|
| Eugia Pharma Specialities Limited | Sangareddy, India | Makes it, tests it and packages it | Serious problems, FDA actionFeb 6, 2026 · 7 inspections, 2 with FDA action |
Repackaging site
- HF Acquisition Co LLC, Mukilteo, WA, United States · relabels it
Product details
- Generic drug
- Vasopressin, Unspecified: every company that makes it
- Form
- injection, intravenous
- Strength
- 20 [USP'U] per 1 mL
- Approval
- ANDA ANDA214314
- On the market since
- Mar 2, 2023
- Package NDCs
51662-1623-151662-1623-2- Official label
- DailyMed (National Library of Medicine), updated Jul 11, 2025
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