United States · FDA National Drug Code directory
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A source-listed medicine record.
Factual source checks only. This page is not a clinically reviewed monograph. Historical or discontinued records may be included; listing does not confirm approval, current availability or pharmacy stock.
Medicine identity
- Source reference
- 64842-1020_15b86e86-8940-44e3-921c-2e0b97180ea1
- Product NDC
- 64842-1020
- Form
- TABLET, FILM COATED
- Composition / generic term
- trifluridine and tipiracil
- Labeler
- Taiho Pharmaceutical Co., Ltd.
- Marketing category
- NDA
- Marketing start / end (source format)
- 20150922
- Source listing expiry
- 20261231
Source-listed ingredients
- TRIFLURIDINE — 20 mg/1
- TIPIRACIL HYDROCHLORIDE — 8.19 mg/1
These values do not establish equivalence or a dose recommendation.
Packages
- 20 TABLET, FILM COATED in 1 BOTTLE (64842-1020-1) · 64842-1020-1
- 40 TABLET, FILM COATED in 1 BOTTLE (64842-1020-2) · 64842-1020-2
- 60 TABLET, FILM COATED in 1 BOTTLE (64842-1020-3) · 64842-1020-3
Source and coverage
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Snapshot retrieved: 2026-09-17. This is the acquisition date, not a medical review date.
Clinical information, images and comparisons appear only when separately reviewed for this record. Coverage may be incomplete. Ask a pharmacist or clinician about your treatment.
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