51167-548 : Journavx 50 mg Oral Tablet, Film Coated


NDC: 51167-548
Labeler: Vertex Pharmaceuticals Incorporated
Product Type: Human Prescription Drug
Drug Name:  Journavx
Dosage Form: Oral Tablet, Film Coated
Application #: NDA219209
Rev. Date: 


NDC Package Codes:

  • 51167-548-25: 5 BLISTER PACK IN 1 CARTON (51167‑548‑25) / 5 TABLET, FILM COATED IN 1 BLISTER PACK (51167‑548‑05)
  • 51167-548-30: 30 TABLET, FILM COATED IN 1 BOTTLE (51167‑548‑30)
  • 51167-548-31: 100 TABLET, FILM COATED IN 1 BOTTLE (51167‑548‑31)
  • 51167-548-34: 10 BLISTER PACK IN 1 CARTON (51167‑548‑34) / 10 TABLET, FILM COATED IN 1 BLISTER PACK

Active Ingredients:

  • Suzetrigine

Dosage Strength:

  • 50 mg

Pharmaceutical Classes:

  • Cytochrome P450 3A Inducers [MoA]
  • Sodium Channel Antagonists [MoA]
  • Sodium Channel Blocker [EPC]

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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.