64842-1025 : Lonsurf Oral Tablet, Film Coated


NDC64842-1025
Labeler: Taiho Pharmaceutical Co., Ltd.
Product Type: Human Prescription Drug
Drug Name:  Lonsurf
Dosage Form: Oral Tablet, Film Coated
Application #: NDA207981
Rev. Date: 


Appearance:


Markings: 15;102;15;mg
Shapes:  Round
Colors:  White
Size (mm): 7
Segments: * 1

* Segments = the number of equally sized pieces which the pill can be broken into. In this case, a value of 1 indicates a solid pill with no score lines.

NDC Package Codes:

  • 64842-1025-1: 20 TABLET, FILM COATED IN 1 BOTTLE (64842‑1025‑1)
  • 64842-1025-2: 40 TABLET, FILM COATED IN 1 BOTTLE (64842‑1025‑2)
  • 64842-1025-3: 60 TABLET, FILM COATED IN 1 BOTTLE (64842‑1025‑3)

Active Ingredients:

  • Trifluridine
  • Tipiracil Hydrochloride

Dosage Strength:

  • 15 mg
  • 6.14 mg

Inactive Ingredients:

  • Alcohol
  • Butyl Alcohol

Pharmaceutical Classes:

  • Nucleoside Analog [EXT]
  • Nucleoside Analog Antiviral [EPC]
  • Nucleoside Metabolic Inhibitor [EPC]
  • Nucleic Acid Synthesis Inhibitors [MoA]
  • Thymidine Phosphorylase Inhibitor [EPC]
  • Thymidine Phosphorylase Inhibitors [MoA]

Related Products:

Based on records with the same trade name.
  • 64842-1020 Lonsurf Oral Tablet, Film Coated by Taiho Pharmaceutical Co., Ltd.

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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.