NDC 23155-833
Hydralazine Hydrochloride 25 mg tablet
On the label: Heritage Pharmaceuticals Inc. d/b/a Avet Pharmaceuticals Inc..
Where it's made
| Factory | Where | Role | Last FDA inspection |
|---|---|---|---|
| Heritage Pharma Labs Inc. d/b/a Avet Pharmaceuticals Labs Inc. | East Brunswick, NJ, United States | Makes it, tests it and packages it | No problems foundSep 19, 2023 · 10 inspections |
| Stallion Laboratories Private Limited | Ahmedabad, India | Makes it, tests it and packages it | Problems found, fixed voluntarilyJul 12, 2024 · 1 inspection |
Product details
- Generic drug
- Hydralazine: every company that makes it
- Form
- tablet, oral
- Strength
- 25 mg
- Approval
- ANDA ANDA040858
- On the market since
- Aug 2, 2023
- Package NDCs
23155-833-0123155-833-10- Official label
- DailyMed (National Library of Medicine), updated Apr 3, 2026
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