Drugplain

LONSURF 6.14 mg/1

trifluridine and tipiracil · TABLET, FILM COATED · Taiho Pharmaceutical Co., Ltd.

No Recall History
Plain English

LONSURF is a tablet, film coated containing trifluridine and tipiracil at 6.14 mg/1, taken oral. Manufactured by Taiho Pharmaceutical Co., Ltd..

Key Facts

Brand Name
LONSURF
Generic Name
trifluridine and tipiracil
NDC Code (Product)
64842-1025
Manufacturer
Taiho Pharmaceutical Co., Ltd.
Strength
6.14 mg/1
Dosage Form
TABLET, FILM COATED
Route
ORAL
Marketing Status
Application #
NDA207981
Drug Class
Nucleoside Analog Antiviral [EPC]; Nucleoside Metabolic Inhibitor [EPC]
Marketing Start
09/22/2015

Recall History

No Recall History

Frequently Asked Questions

What is LONSURF used for?

LONSURF contains trifluridine and tipiracil. It is a tablet, film coated taken oral. Consult your doctor for specific uses.

Is LONSURF a controlled substance?

LONSURF is not classified as a controlled substance by the DEA.

What is the generic name for LONSURF?

The generic name for LONSURF is trifluridine and tipiracil. There are no other listed brand versions of trifluridine and tipiracil.

What is the NDC code for LONSURF 6.14 mg/1?

The NDC (National Drug Code) for LONSURF 6.14 mg/1 is 64842-1025, listed by Taiho Pharmaceutical Co., Ltd..

Product NDC

64842-1025

Package NDC

64842-1025-1

Other LONSURF Dosages

Not medical advice. Always consult your doctor or pharmacist before making any medication decisions.

Data from openFDA · Public domain (CC0 1.0)