# AUVELITY

NDC: 81968-345
Generic name: dextromethorphan hydrobromide, bupropion hydrochloride
Labeler / Manufacturer: Axsome Therapeutics, Inc.
Product type: HUMAN PRESCRIPTION DRUG
Marketing category: New Drug Application (innovator)
Dosage form: KIT
Routes: —
Marketing started: 20260601

FDA application: NDA215430

## Active ingredients

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## Pharmacological class

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## External sources

- openFDA: https://api.fda.gov/drug/ndc.json?search=product_ndc:"81968-345"
- FDA NDC Directory: https://www.accessdata.fda.gov/scripts/cder/ndc/dsp_searchresult.cfm?p_ndc=81968-345
- DailyMed: https://dailymed.nlm.nih.gov/dailymed/lookup.cfm?setid=dcefda7c-9a68-278e-e053-2995a90aec79