81968-045 : Auvelity Oral Tablet, Multilayer, Extended Release


NDC: 81968-045
Labeler: Axsome Therapeutics, Inc.
Product Type: Human Prescription Drug
Drug Name:  Auvelity
Dosage Form: Oral Tablet, Multilayer, Extended Release
Application #: NDA215430
Rev. Date: 


NDC Package Codes:

  • 81968-045-14: 1 BOTTLE IN 1 CARTON (81968‑045‑14) / 14 TABLET, MULTILAYER, EXTENDED RELEASE IN 1 BOTTLE
  • 81968-045-30: 30 TABLET, MULTILAYER, EXTENDED RELEASE IN 1 BOTTLE (81968‑045‑30)
  • 81968-045-31: 1 BOTTLE IN 1 CARTON (81968‑045‑31) / 30 TABLET, MULTILAYER, EXTENDED RELEASE IN 1 BOTTLE
  • 81968-045-60: 60 TABLET, MULTILAYER, EXTENDED RELEASE IN 1 BOTTLE (81968‑045‑60)

Active Ingredients:

  • Bupropion Hydrochloride
  • Dextromethorphan Hydrobromide

Dosage Strength:

  • 105 mg
  • 45 mg

Pharmaceutical Classes:

  • Aminoketone [EPC]
  • Dopamine Uptake Inhibitors [MoA]
  • Increased Dopamine Activity [PE]
  • Increased Norepinephrine Activity [PE]
  • Norepinephrine Uptake Inhibitors [MoA]
  • Sigma-1 Agonist [EPC]
  • Sigma-1 Receptor Agonists [MoA]
  • Uncompetitive N-methyl-D-aspartate Receptor Antagonist [EPC]
  • Uncompetitive NMDA Receptor Antagonists [MoA]

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Note: The RxChat NDC Database uses publicly available data from the FDA and the U.S. National Library of Medicine (NLM); The NLM is not responsible for the data presented and does not endorse or recommend this or any other product. While we make every effort to ensure that the information presented is accurate, you should assume that all results are unvalidated. To report any errors or inconsistencies please contact us.