LONSURF (Taiho Pharmaceutical Co., Ltd.)


Welcome to the PulseAid listing for the LONSURF drug offered from Taiho Pharmaceutical Co., Ltd.. This Nucleoside Analog [Chemical/Ingredient],Nucleoside Analog Antiviral [EPC],Nucleoside Metabolic Inhibitor [EPC],Nucleic Acid Synthesis Inhibitors [MoA],Thymidine Phosphorylase Inhibitor [EPC],Thymidine Phosphorylase Inhibitors [MoA] pharmaceutical is classified as a HUMAN PRESCRIPTION DRUG. Below, you can view details for this drug, such as its dosage form, route of delivery, start market/end market dates, and more. We have also randomly listed additional pharmaceuticals used in the same HUMAN PRESCRIPTION DRUG drug type category.
LABELER NAME / MANUFACTURER: Taiho Pharmaceutical Co., Ltd.
NON-PROPRIETARY NAME: trifluridine and tipiracil
SUBSTANCE NAME: TRIFLURIDINE; TIPIRACIL HYDROCHLORIDE
TYPE: HUMAN PRESCRIPTION DRUG
PHARMA CLASS: Nucleoside Analog [Chemical/Ingredient],Nucleoside Analog Antiviral [EPC],Nucleoside Metabolic Inhibitor [EPC],Nucleic Acid Synthesis Inhibitors [MoA],Thymidine Phosphorylase Inhibitor [EPC],Thymidine Phosphorylase Inhibitors [MoA]
ROUTE: ORAL
DOSAGE FORM: TABLET, FILM COATED
MARKETING CATEGORY NAME: NDA
START MARKETING DATE: 2015-09-22
END MARKETING DATE: 0000-00-00


LONSURF HUMAN PRESCRIPTION DRUG Details:

Item DescriptionLONSURF from Taiho Pharmaceutical Co., Ltd.
LABELER NAME: Taiho Pharmaceutical Co., Ltd.
DEA SCHEDULE:
ACTIVE STRENGTH: 20; 8.19(mg/1; mg/1)
START MARKETING DATE: 2015-09-22
END MARKETING DATE: 0000-00-00
PRODUCT ID: 64842-1020_89fdcc48-8005-487d-828d-93d9ecb94f76
PRODUCT NDC: 64842-1020
APPLICATION NUMBER: NDA207981

Other TRIFLURIDINE; TIPIRACIL HYDROCHLORIDE Pharmaceutical Manufacturers / Labelers:

Manufacturer / LabelerProprietary Name
Taiho Pharmaceutical Co., Ltd.LONSURF