NDC 0517-0901
Hydralazine Hydrochloride 20 mg per 1 mL injection, solution
On the label: American Regent, Inc..
Where it's 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 |
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
0517-0901-25- Official label
- DailyMed (National Library of Medicine), updated May 6, 2019
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