NDC 51662-1682
Vasopressin 20 [USP'U] per 1 mL injection, solution
On the label: HF Acquisition Co. LLC. DBA HealthFirst. It's repackaged: HF Acquisition Co. LLC. DBA HealthFirst rebottles it from American Regent, Inc.'s NDC 0517-1030.
Where the pills inside were made
| Factory | Where | Role | Last FDA inspection |
|---|---|---|---|
| American Regent, Inc. | Hilliard, OH, United States | Makes it | Problems found, fixed voluntarilyJun 18, 2026 · 8 inspections |
Repackaging site
- HF Acquisition Co LLC, Mukilteo, WA, United States · relabels it
Recalls
- May 13, 2024 · Class II · American Regent, Inc.
Subpotent product in addition to having out-of-specification results for impurities.
Lots: Lot #: 23061L1C0, Exp 1/31/2025
Class I recalls are the most serious; Class III the least. A recall covers specific lots, listed on each recall.
Product details
- Generic drug
- Vasopressin: every company that makes it
- Form
- injection, solution, intravenous
- Strength
- 20 [USP'U] per 1 mL
- Approval
- NDA NDA212593
- On the market since
- Jun 21, 2023
- Package NDCs
51662-1682-151662-1682-2- Official label
- DailyMed (National Library of Medicine), updated Jul 21, 2026
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