Taiho Oncology
FDA Approved Drugs

Taiho Oncology

FDA Approved Drugs Database

FDA approved drug product records including application numbers, product numbers, drug names, active ingredients, dosage forms, strengths, approval dates and regulatory status.

RX Discontinued
  • Total Records 5
  • Latest Approval Date Jul 28, 2025
  • Data Source FDA
  • First Approval Date Sep 22, 2015
All
5
View
Discontinued
1
View
RX
4
View
Company Overview

Company

Taiho Oncology

Country

U.S.A

Email

Social Profiles

Company Snapshot

Taiho Oncology

101 Carnegie Center, Suite 101 Princeton, New Jersey 08540

U.S.A

www.taihooncology.com/us/ View on Map
FDA Approved Drug Records ( 5 records )
2020
07 Jul
RX Application: 212576

Drug Name

INQOVI

Product Number

1

Dosage Form

-

Strength

100MG;35MG

Approval Date

2020-07-07

212576 / 1

Active Ingredient

CEDAZURIDINE; DECITABINE

Application Number

212576

Product Number

1

Dosage Form

-

Strength

100MG;35MG

Approval Date

2020-07-07

Regulatory Status

RX

2015
22 Sep
RX Application: 207981

Drug Name

LONSURF

Product Number

1

Dosage Form

-

Strength

EQ 6.14MG BASE;15MG

Approval Date

2015-09-22

207981 / 1

Active Ingredient

TIPIRACIL HYDROCHLORIDE; TRIFLURIDINE

Application Number

207981

Product Number

1

Dosage Form

-

Strength

EQ 6.14MG BASE;15MG

Approval Date

2015-09-22

Regulatory Status

RX

2015
22 Sep
RX Application: 207981

Drug Name

LONSURF

Product Number

2

Dosage Form

-

Strength

EQ 8.19MG BASE;20MG

Approval Date

2015-09-22

207981 / 2

Active Ingredient

TIPIRACIL HYDROCHLORIDE; TRIFLURIDINE

Application Number

207981

Product Number

2

Dosage Form

-

Strength

EQ 8.19MG BASE;20MG

Approval Date

2015-09-22

Regulatory Status

RX

2022
30 Sep
RX Application: 214801

Drug Name

LYTGOBI

Product Number

1

Dosage Form

-

Strength

4MG

Approval Date

2022-09-30

214801 / 1

Active Ingredient

FUTIBATINIB

Application Number

214801

Product Number

1

Dosage Form

-

Strength

4MG

Approval Date

2022-09-30

Regulatory Status

RX

2025
28 Jul
Discontinued Application: 214801

Drug Name

LYTGOBI

Product Number

2

Dosage Form

-

Strength

16MG

Approval Date

2025-07-28

214801 / 2

Active Ingredient

FUTIBATINIB

Application Number

214801

Product Number

2

Dosage Form

-

Strength

16MG

Approval Date

2025-07-28

Regulatory Status

Discontinued

Related Databases
  • FDA Inspections
    0 View
  • EDQM CEP
    0 View
  • KDMF
    0 View
  • Japan DMF
    0 View
  • Eudra GMP
    0 View
  • NDC Database
    0 View
  • FDA Approved Drugs Database
    5 View
  • Drug Prices in Switzerland
    0 View
Drug Status Breakdown
5 total
  • RX
  • Discontinued
Official Source

FDA approved drug data is based on publicly available U.S. Food and Drug Administration Orange Book information.

Visit FDA Orange Book
FDA Approved Drug Record Details Preview

Explore important FDA approved drug information available in the records above.

Drug Name

INQOVI

Application Number

212576

Product Number

1

Active Ingredient

CEDAZURIDINE; DECITABINE

Dosage Form

-

Strength

100MG;35MG

FDA Approved Drug Data

Approved drug product information

Regular Updates

Data maintained from official sources

Structured Database

Searchable pharmaceutical data

Reliable Data

Organized FDA drug records

Create a New Buying Request

Fields marked with * are mandatory.

Please enter quantity.
Please select a unit.
Please select quality standard.
Please select request type.
Please provide product specifications.
Please enter additional details.
Please select shipping preference.
Notice: By submitting this buying request, the provided product details and requirements may be published publicly on our marketplace.