What are the active and inactive ingredients in Auvelity (dextromethorphan/bupropion) tablets?

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Last updated: November 12, 2026 • View editorial policy

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Auvelity Composition

Auvelity contains two active ingredients: dextromethorphan hydrobromide 45 mg (immediate-release) and bupropion hydrochloride 105 mg (extended-release) in each tablet. 1

Active Ingredients

  • Dextromethorphan hydrobromide: 45 mg per tablet (equivalent to 32.98 mg dextromethorphan base) in an immediate-release formulation
  • Bupropion hydrochloride: 105 mg per tablet (equivalent to 91.14 mg bupropion base) in an extended-release formulation

The combination is designed so that bupropion inhibits CYP2D6, which prevents the rapid metabolism of dextromethorphan, thereby increasing its bioavailability and therapeutic levels 1, 2.

Inactive Ingredients

Each tablet contains the following inactive excipients 1:

  • L-cysteine hydrochloride monohydrate
  • Carbomer homopolymer
  • Microcrystalline cellulose
  • Colloidal silicon dioxide
  • Crospovidone
  • Stearic acid
  • Magnesium stearate
  • Glyceryl monocaprylocaprate
  • Polyvinyl alcohol
  • Sodium lauryl sulfate
  • Talc
  • Titanium dioxide
  • Red iron oxide
  • Yellow iron oxide

Mechanism of Action

Dextromethorphan acts as an uncompetitive NMDA receptor antagonist and sigma-1 receptor agonist, while bupropion functions as a norepinephrine/dopamine reuptake inhibitor and CYP2D6 inhibitor 1, 2. The bupropion component serves a dual purpose: it provides antidepressant effects through noradrenergic and dopaminergic mechanisms, and it competitively inhibits the metabolism of dextromethorphan, preventing its conversion to dextrorphan (which has mu-opioid agonist properties) 3.

Formulation Details

The medication is formulated as round bilayer tablets for oral administration, with the dextromethorphan in an immediate-release layer and bupropion in an extended-release layer 1. This specific formulation design allows for the pharmacokinetic synergy between the two components, where bupropion maintains consistent dextromethorphan levels throughout the dosing interval 3.

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This information is intended for healthcare professionals. Any medical decision-making should rely on clinical judgment and independently verified information. The content provided herein does not replace professional discretion and should be considered supplementary to established clinical guidelines. Healthcare providers should verify all information against primary literature and current practice standards before application in patient care. Dr.Oracle assumes no liability for clinical decisions based on this content.