0173-0922 : Blujepa 750 mg Oral Tablet, Film Coated


NDC: 0173-0922
Labeler: Glaxosmithkline LLC
Product Type: Human Prescription Drug
Drug Name:  Blujepa
Dosage Form: Oral Tablet, Film Coated
Application #: NDA218230
Rev. Date: 


NDC Package Codes:

  • 0173-0922-38: 8 TABLET, FILM COATED IN 1 BOTTLE (0173‑0922‑38)
  • 0173-0922-45: 20 TABLET, FILM COATED IN 1 BOTTLE (0173‑0922‑45)

Active Ingredients:

  • Gepotidacin Mesylate

Dosage Strength:

  • 750 mg

Pharmaceutical Classes:

  • Cholinesterase Inhibitors [MoA]
  • Cytochrome P450 3A4 Inhibitors [MoA]
  • P-Glycoprotein Inhibitors [MoA]
  • Topoisomerase 2 Inhibitors [MoA]
  • Topoisomerase 4 Inhibitors [MoA]
  • Triazaacenaphthylene Bacterial Type II Topoisomerase Inhibitor [EPC]

NDC QR Code

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NDC 0173-0922 QR Code

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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.