NDC 87063-309
Modafinil 200 mg tablet
On the label: Asclemed USA, Inc.. It's repackaged: Asclemed USA, Inc. rebottles it from Viona Pharmaceuticals Inc.'s NDC 72578-006.
Where the pills inside were made
| Factory | Where | Role | Last FDA inspection |
|---|---|---|---|
| Zydus Lifesciences Limited | Ahmedabad, India | Makes it and tests it | Problems found, fixed voluntarilyMar 24, 2023 · 5 inspections |
Repackaging site
- Asclemed USA Inc. dba Enovachem, Torrance, CA, United States · repackages it and relabels it
Product details
- Generic drug
- Modafinil: every company that makes it
- Form
- tablet, oral
- Strength
- 200 mg
- Approval
- ANDA ANDA209966
- On the market since
- Feb 15, 2019
- Package NDCs
87063-309-0187063-309-3087063-309-6087063-309-90- Official label
- DailyMed (National Library of Medicine), updated Sep 10, 2026
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