NDC 60687-294
Voriconazole 50 mg tablet, film coated
On the label: American Health Packaging. It's repackaged: American Health Packaging rebottles it from Glenmark Pharmaceuticals Inc., USA's NDC 68462-572.
Where the pills inside were made
| Factory | Where | Role | Last FDA inspection |
|---|---|---|---|
| Glenmark Pharmaceuticals Limited | Dhar, India | Makes it and tests it | Serious problems, FDA actionFeb 14, 2025 · 8 inspections, 1 with FDA action |
Repackaging site
- American Health Packaging, Columbus, OH, United States · repackages it
Recalls
- Mar 24, 2025 · Class II · Amerisource Health Services LLC
cGMP Deviations: Received notification from their supplier requesting they perform a recall due to the fact they repackaged the product.
Lots: Lot # 1014138, Exp 04/30/2025 - Mar 13, 2025 · Class II · Glenmark Pharmaceuticals Inc., USA
CGMP Deviations
Lots: Lot # 17230853, exp. date Mar-25 17231271, exp. date May-25 17231300, exp. date May-25 17242050, exp. date Oct-26 17231046, exp. date Apr-25 17241156, exp. date Jun-26 17241388, exp. date Jul-26 17241800, exp. date Sep-26 - Mar 13, 2025 · Class II · Glenmark Pharmaceuticals Inc., USA
CGMP Deviations
Lots: Lot # 17231045, exp. date Apr-25
Class I recalls are the most serious; Class III the least. A recall covers specific lots, listed on each recall.
Product details
- Generic drug
- Voriconazole: every company that makes it
- Form
- tablet, film coated
- Strength
- 50 mg
- Approval
- ANDA ANDA203503
- On the market since
- Mar 7, 2018
- Package NDCs
60687-294-1160687-294-21- Official label
- DailyMed (National Library of Medicine), updated Sep 18, 2025
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