NDC 51662-1648
Hydralazine Hydrochloride 20 mg 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 0517-0901.
Where the pills inside were made
| Factory | Where | Role | Last FDA inspection |
|---|---|---|---|
| American Regent, Inc. | Shirley, NY, United States | Makes it, tests it and sterilizes it | Problems found, fixed voluntarilyApr 24, 2024 · 12 inspections, 1 with FDA action |
Repackaging site
- HF Acquisition Co LLC, Mukilteo, WA, United States · relabels it
Product details
- Generic drug
- Hydralazine: every company that makes it
- Form
- injection, solution, intramuscular; intravenous
- Strength
- 20 mg per 1 mL
- Approval
- ANDA ANDA040136
- On the market since
- Jun 30, 1997
- Package NDCs
51662-1648-251662-1648-3- Official label
- DailyMed (National Library of Medicine), updated Apr 9, 2024
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