NDC 72319-012
isosorbide dinitrate and hydralazine hydrochloride 20 mg / 37.5 mg tablet, film coated
On the label: i3 Pharmaceuticals, LLC.
Where it's made
| Factory | Where | Role | Last FDA inspection |
|---|---|---|---|
| i3 Pharmaceuticals, LLC | Warminster, PA, United States | Makes it and packages it | Problems found, fixed voluntarilyMay 22, 2026 · 4 inspections |
Product details
- Generic drug
- Hydralazine and Isosorbide Dinitrate: every company that makes it
- Form
- tablet, film coated, oral
- Strength
- 20 mg / 37.5 mg
- Approval
- ANDA ANDA215988
- On the market since
- Feb 7, 2024
- Package NDCs
72319-012-0372319-012-18- Official label
- DailyMed (National Library of Medicine), updated May 16, 2024
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