63379-039 : Treximet Oral Tablet, Film Coated

Labeler: Glaxo Operations Uk Ltd
Product Type: Human Prescription Drug
Drug Name:  Treximet
Dosage Form: Oral Tablet, Film Coated
Application #: NDA021926
Rev. Date: 

NDC Package Codes:

  • 63379-039-00: 1 TABLET, FILM COATED IN 1 BOTTLE (63379‑039‑00)
  • 63379-039-01: 9 TABLET, FILM COATED IN 1 BOTTLE (63379‑039‑01)
  • 63379-039-02: 9 TABLET, FILM COATED IN 1 CONTAINER (63379‑039‑02)

Active Ingredients:

  • Sumatriptan Succinate
  • Naproxen Sodium

Dosage Strength:

  • 85 mg
  • 500 mg

Pharmaceutical Classes:

  • Serotonin 1b Receptor Agonists [MoA]
  • Serotonin 1d Receptor Agonists [MoA]
  • Serotonin-1b and Serotonin-1d Receptor Agonist [EPC]
  • Cyclooxygenase Inhibitors [MoA]
  • Nonsteroidal Anti-inflammatory Compounds [Chemical/Ingredient]
  • Nonsteroidal Anti-inflammatory Drug [EPC]

Related Products:

Based on records with the same trade name.
  • 0173-0750 Treximet 85/500 (Sumitriptan / Naproxen Sodium) Oral Tablet by Glaxosmithkline LLC
  • 21695-954 Treximet 85/500 (Sumitriptan / Naproxen Sodium) Oral Tablet by Rebel Distributors Corp
  • 42847-850 Treximet Oral Tablet, Film Coated by Currax Pharmaceuticals LLC
  • 65224-850 Treximet Oral Tablet, Film Coated by Pernix Therapeutics
  • 65224-860 Treximet Oral Tablet, Film Coated by Pernix Therapeutics


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Note: The MedsChat® 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.