NDC 72572-265
Hydralazine Hydrochloride 20 mg per 1 mL injection, solution
On the label: Civica, Inc..
Where it's made
| Factory | Where | Role | Last FDA inspection |
|---|---|---|---|
| American Regent, Inc. | Shirley, NY, United States | Makes it and tests 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
- Oct 29, 2020
- Package NDCs
72572-265-0172572-265-25- Official label
- DailyMed (National Library of Medicine), updated Apr 28, 2024
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