NDC 43066-041
Hydralazine Hydrochloride 20 mg per 1 mL injection
On the label: Baxter Healthcare Corporation.
Where it's made
| Factory | Where | Role | Last FDA inspection |
|---|---|---|---|
| Immacule Lifesciences Private Limited | Solan, India | Makes it, tests it, packages it, labels it and sterilizes it | Serious problems, FDA actionSep 18, 2025 · 3 inspections, 1 with FDA action |
Product details
- Generic drug
- Hydralazine: every company that makes it
- Form
- injection, intramuscular; intravenous
- Strength
- 20 mg per 1 mL
- Approval
- ANDA ANDA219797
- On the market since
- Jul 17, 2025
- Package NDCs
43066-041-0143066-041-25- Official label
- DailyMed (National Library of Medicine), updated Mar 10, 2025
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