NDC 68151-2701
Quinidine Gluconate 324 mg tablet, extended release
On the label: Carilion Materials Management. It's repackaged: Carilion Materials Management rebottles it from Caraco Pharmaceutical Laboratories, Ltd.'s NDC 53489-141.
Where the pills inside were made
| Factory | Where | Role | Last FDA inspection |
|---|---|---|---|
| Frontida BioPharm, LLC | Philadelphia, PA, United States | Makes it, tests it and packages it | No problems foundApr 2, 2026 · 10 inspections, 1 with FDA action |
Repackaging site
- Carilion Materials Management, Roanoke, Virginia, United States · repackages it
Product details
- Generic drug
- Quinidine: every company that makes it
- Form
- tablet, extended release
- Strength
- 324 mg
- Approval
- ANDA ANDA089338
- On the market since
- Feb 10, 1987
- Package NDCs
68151-2701-0- Official label
- DailyMed (National Library of Medicine), updated Aug 4, 2016
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