NDC 50268-571
Modafinil 200 mg tablet
On the label: AvPAK. It's repackaged: AvPAK 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 |
Product details
- Generic drug
- Modafinil: every company that makes it
- Form
- tablet, oral
- Strength
- 200 mg
- Approval
- ANDA ANDA202566
- On the market since
- Aug 1, 2016
- Package NDCs
50268-571-1150268-571-12- Official label
- DailyMed (National Library of Medicine), updated Jun 2, 2022
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