NDC 71610-913
Zolpidem Tartrate 6.25 mg tablet, film coated, extended release
On the label: Aphena Pharma Solutions - Tennessee, Inc.. It's repackaged: Aphena Pharma Solutions - Tennessee, Inc. rebottles it from Caraco Pharmaceutical Laboratories, Ltd.'s NDC 47335-307.
Where the pills inside were made
| Factory | Where | Role | Last FDA inspection |
|---|---|---|---|
| Sun Pharmaceutical Industries Limited | Dadra, India | Makes it and tests it | Problems found, fixed voluntarilyMar 29, 2019 · 5 inspections |
Repackaging site
- Aphena Pharma Solutions - Tennessee, LLC, Cookeville, TN, United States · repackages it
Recalls
- Jan 18, 2024 · Class II · Sun Pharmaceutical Industries Inc
CGMP Deviations: Microbial contamination was reported in stagnant water in the duct of the manufacturing equipment.
Lots: Lot #: DNE0892A Exp. 07/31/2026 - Jan 18, 2024 · Class II · Sun Pharmaceutical Industries Inc
CGMP Deviations: Microbial contamination was reported in stagnant water in the duct of the manufacturing equipment.
Lots: Lot #: DNE0893A Expires 07/31/2026
Class I recalls are the most serious; Class III the least. A recall covers specific lots, listed on each recall.
Product details
- Generic drug
- Zolpidem: every company that makes it
- Form
- tablet, film coated, extended release, oral
- Strength
- 6.25 mg
- Approval
- ANDA ANDA204170
- On the market since
- May 15, 2017
- Package NDCs
71610-913-3071610-913-5371610-913-60- Official label
- DailyMed (National Library of Medicine), updated Jun 9, 2025
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