NDC 64842-1020
Lonsurf 20 mg / 8.19 mg tablet, film coated
On the label: Taiho Pharmaceutical Co., Ltd..
Where it's made
| Factory | Where | Role | Last FDA inspection |
|---|---|---|---|
| Ajinomoto Co., Inc. | Yokkaichi, Japan | Makes the active ingredient and tests it | Problems found, fixed voluntarilyNov 14, 2025 · 3 inspections |
| Taiho Pharmaceutical Co., Ltd. | Kodama-gun, Japan | Makes the active ingredient and tests it | No problems foundOct 13, 2023 · 2 inspections |
| Taiho Pharmaceutical Co., Ltd. | Itano-gun, Japan | Makes it and tests it | Problems found, fixed voluntarilyJan 26, 2024 · 2 inspections |
| Yuki Gosei Kogyo Co., Ltd. | Iwaki, Japan | Makes the active ingredient | Problems found, fixed voluntarilyFeb 6, 2026 · 7 inspections, 2 with FDA action |
Product details
- Generic drug
- Tipiracil and Trifluridine: every company that makes it
- Form
- tablet, film coated, oral
- Strength
- 20 mg / 8.19 mg
- Approval
- NDA NDA207981
- On the market since
- Sep 22, 2015
- Package NDCs
64842-1020-164842-1020-264842-1020-3- Official label
- DailyMed (National Library of Medicine), updated Nov 5, 2025
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