NDC 70518-3852
Hydralazine Hydrochloride 25 mg tablet
On the label: Remedyrepack Inc.. It's repackaged: Remedyrepack Inc. rebottles it from ScieGen Pharmaceuticals, Inc.'s NDC 50228-183.
Where the pills inside were made
| Factory | Where | Role | Last FDA inspection |
|---|---|---|---|
| ScieGen Pharmaceuticals, INC. | Hauppauge, NY, United States | Makes it and tests it | Problems found, fixed voluntarilyMay 15, 2026 · 15 inspections, 1 with FDA action |
Product details
- Generic drug
- Hydralazine: every company that makes it
- Form
- tablet, oral
- Strength
- 25 mg
- Approval
- ANDA ANDA205236
- On the market since
- Sep 3, 2023
- Package NDCs
70518-3852-0- Official label
- DailyMed (National Library of Medicine), updated Jun 9, 2026
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