NDC 68084-721
Modafinil 200 mg tablet
On the label: American Health Packaging. It's repackaged: American Health Packaging rebottles it from Aurobindo Pharma Limited's NDC 65862-602.
Where the pills inside were made
| Factory | Where | Role | Last FDA inspection |
|---|---|---|---|
| Apl Healthcare Limited | Mahabubnagar, India | Makes it and tests it | No problems foundJan 18, 2023 · 2 inspections |
| 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
- Modafinil: every company that makes it
- Form
- tablet, oral
- Strength
- 200 mg
- Approval
- ANDA ANDA202566
- On the market since
- Jun 2, 2014
- Package NDCs
68084-721-1168084-721-21- Official label
- DailyMed (National Library of Medicine), updated Oct 31, 2024
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