NDC 51662-1694
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 Dr. Reddy's Laboratories Inc.'s NDC 43598-914.
Where the pills inside were made
| Factory | Where | Role | Last FDA inspection |
|---|---|---|---|
| Dr.reddy's Laboratories Limited | Visakhapatnam, India | Makes it, tests it and packages it | Problems found, fixed voluntarilyMay 17, 2024 · 9 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 ANDA213988
- On the market since
- May 9, 2024
- Package NDCs
51662-1694-151662-1694-2- Official label
- DailyMed (National Library of Medicine), updated Aug 17, 2026
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