NDC 60687-549
Ranolazine 500 mg tablet, extended release
On the label: American Health Packaging. It's repackaged: American Health Packaging rebottles it from Ajanta Pharma USA Inc.'s NDC 27241-125.
Where the pills inside were made
| Factory | Where | Role | Last FDA inspection |
|---|---|---|---|
| Ajanta Pharma Limited | Bharuch, India | Makes it | No problems foundJun 23, 2023 · 3 inspections |
Repackaging site
- American Health Packaging, Columbus, OH, United States · repackages it
Recalls
- Sep 17, 2026 · Class II · Ajanta Pharma USA Inc
Failed Dissolution Specifications: below specification
Lots: Lot: DJ25134, Exp 11/30/2028
Class I recalls are the most serious; Class III the least. A recall covers specific lots, listed on each recall.
Product details
- Generic drug
- Ranolazine: every company that makes it
- Form
- tablet, extended release, oral
- Strength
- 500 mg
- Approval
- ANDA ANDA210054
- On the market since
- Aug 19, 2020
- Package NDCs
60687-549-1160687-549-21- Official label
- DailyMed (National Library of Medicine), updated Aug 19, 2026
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