Taiho Oncology Discontinued
FDA Approved Drugs

Taiho Oncology Discontinued

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.

Discontinued
  • Total Records 1
  • Latest Approval Date Jul 28, 2025
  • Data Source FDA
  • First Approval Date Jul 28, 2025
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Discontinued
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RX
4
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Company Overview

Company

Taiho Oncology Discontinued

Country

U.S.A

Email

Social Profiles

Company Snapshot

Taiho Oncology Discontinued

101 Carnegie Center, Suite 101 Princeton, New Jersey 08540

U.S.A

www.taihooncology.com/us/ View on Map
FDA Approved Drug Records ( 1 record )
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

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Drug Status Breakdown
1 total
  • Discontinued
Official Source

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

Drug Name

LYTGOBI

Application Number

214801

Product Number

2

Active Ingredient

FUTIBATINIB

Dosage Form

-

Strength

16MG

FDA Approved Drug Data

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