NDC 60687-968
Voriconazole 50 mg tablet, film coated
On the label: American Health Packaging. It's repackaged: American Health Packaging rebottles it from Aurobindo Pharma Limited's NDC 65862-891.
Where the pills inside were made
| Factory | Where | Role | Last FDA inspection |
|---|---|---|---|
| Aurobindo Pharma Limited | Mahabubnagar, India | Makes it and tests it | Problems found, fixed voluntarilyMay 10, 2022 · 7 inspections, 1 with FDA action |
Repackaging site
- American Health Packaging, Columbus, OH, United States · repackages it
Product details
- Generic drug
- Voriconazole: every company that makes it
- Form
- tablet, film coated, oral
- Strength
- 50 mg
- Approval
- ANDA ANDA206837
- On the market since
- Aug 27, 2026
- Package NDCs
60687-968-1160687-968-21- Official label
- DailyMed (National Library of Medicine), updated Aug 27, 2026
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