# AUVELITY

NDC: 81968-030
Generic name: dextromethorphan hydrobromide, bupropion hydrochloride
Labeler / Manufacturer: Axsome Therapeutics, Inc.
Product type: HUMAN PRESCRIPTION DRUG
Marketing category: New Drug Application (innovator)
Dosage form: TABLET, MULTILAYER, EXTENDED RELEASE
Routes: ORAL
Marketing started: 20260508

FDA application: NDA215430

## Active ingredients

- BUPROPION HYDROCHLORIDE: 105 mg/1
- DEXTROMETHORPHAN HYDROBROMIDE: 30 mg/1

## Pharmacological class

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## External sources

- openFDA: https://api.fda.gov/drug/ndc.json?search=product_ndc:"81968-030"
- FDA NDC Directory: https://www.accessdata.fda.gov/scripts/cder/ndc/dsp_searchresult.cfm?p_ndc=81968-030
- DailyMed: https://dailymed.nlm.nih.gov/dailymed/lookup.cfm?setid=dcefda7c-9a68-278e-e053-2995a90aec79