NDC 81968-030
Auvelity 30 mg / 105 mg tablet, multilayer, extended release
On the label: Axsome Therapeutics, Inc..
Where it's made
| Factory | Where | Role | Last FDA inspection |
|---|---|---|---|
| Dipharma Francis Srl | Baranzate, Italy | Makes the active ingredient | Problems found, fixed voluntarilyJul 15, 2022 · 7 inspections |
| Divi's Laboratories Limited | Yadadri Bhuvanagiri District, India | Makes the active ingredient | No problems foundNov 14, 2025 · 5 inspections |
| Patheon Inc. | Whitby, Canada | Makes it | Problems found, fixed voluntarilyFeb 17, 2023 · 8 inspections |
Product details
- Generic drug
- Bupropion and Dextromethorphan: every company that makes it
- Form
- tablet, multilayer, extended release, oral
- Strength
- 30 mg / 105 mg
- Approval
- NDA NDA215430
- On the market since
- May 8, 2026
- Package NDCs
81968-030-22- Official label
- DailyMed (National Library of Medicine), updated Aug 17, 2026
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