NDC 81968-045-30
AUVELITY 105 mg/1
dextromethorphan hydrobromide, bupropion hydrochloride · TABLET, MULTILAYER, EXTENDED RELEASE
AUVELITY is a tablet, multilayer, extended release containing dextromethorphan hydrobromide, bupropion hydrochloride at a strength of 105 mg/1. Manufactured by Axsome Therapeutics, Inc..
Key Facts
- Brand Name
- AUVELITY
- Generic Name
- dextromethorphan hydrobromide, bupropion hydrochloride
- NDC Code (Package)
81968-045-30- NDC Code (Product)
81968-045- Manufacturer
- Axsome Therapeutics, Inc.
- Strength
- 105 mg/1
- Dosage Form
- TABLET, MULTILAYER, EXTENDED RELEASE
- Route
- ORAL
- Marketing Status
- Application #
- NDA215430
- Marketing Start
- 08/18/2022
Recall History
No Recall HistoryView Full Drug Page
AUVELITY — All PackagesNot medical advice. This information is for reference only. Always consult your doctor or pharmacist.