NDC 72319-021
Ranolazine 500 mg tablet, film coated, extended release
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
- Ranolazine: every company that makes it
- Form
- tablet, film coated, extended release, oral
- Strength
- 500 mg
- Approval
- ANDA ANDA213517
- On the market since
- Jun 15, 2022
- Package NDCs
72319-021-02- Official label
- DailyMed (National Library of Medicine), updated May 4, 2022
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