Takeda Pharmaceutical Unclassified
FDA Approved Drugs

Takeda Pharmaceutical Unclassified

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.

Unclassified
  • Total Records 8
  • Latest Approval Date -
  • Data Source FDA
  • First Approval Date -
All
123
View
Unclassified
8
View
Discontinued
31
View
RX
84
View
Company Overview

Company

Takeda Pharmaceutical Unclassified

Country

Japan

Website

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Company Snapshot

Takeda Pharmaceutical Unclassified

1-1, Nihonbashi-Honcho 2-chome, Chuo-ku, Tokyo 103-8668

Japan

www.takeda.com/ View on Map
FDA Approved Drug Records ( 8 records )
-
Unclassified Application: 125476

Drug Name

ENTYVIO

Product Number

1

Dosage Form

-

Strength

300MG

Approval Date

-

125476 / 1

Active Ingredient

VEDOLIZUMAB

Application Number

125476

Product Number

1

Dosage Form

-

Strength

300MG

Approval Date

-

Regulatory Status

Unclassified

-
Unclassified Application: 761133

Drug Name

ENTYVIO

Product Number

1

Dosage Form

-

Strength

300MG

Approval Date

-

761133 / 1

Active Ingredient

VEDOLIZUMAB

Application Number

761133

Product Number

1

Dosage Form

-

Strength

300MG

Approval Date

-

Regulatory Status

Unclassified

-
Unclassified Application: 761133

Drug Name

ENTYVIO

Product Number

2

Dosage Form

-

Strength

108MG/0.68ML

Approval Date

-

761133 / 2

Active Ingredient

VEDOLIZUMAB

Application Number

761133

Product Number

2

Dosage Form

-

Strength

108MG/0.68ML

Approval Date

-

Regulatory Status

Unclassified

-
Unclassified Application: 761359

Drug Name

ENTYVIO

Product Number

1

Dosage Form

-

Strength

300MG

Approval Date

-

761359 / 1

Active Ingredient

VEDOLIZUMAB

Application Number

761359

Product Number

1

Dosage Form

-

Strength

300MG

Approval Date

-

Regulatory Status

Unclassified

-
Unclassified Application: 761359

Drug Name

ENTYVIO

Product Number

2

Dosage Form

-

Strength

108MG/0.68ML

Approval Date

-

761359 / 2

Active Ingredient

VEDOLIZUMAB

Application Number

761359

Product Number

2

Dosage Form

-

Strength

108MG/0.68ML

Approval Date

-

Regulatory Status

Unclassified

-
Unclassified Application: 220860

Drug Name

ORZEYFUL

Product Number

1

Dosage Form

-

Strength

.05MG

Approval Date

-

220860 / 1

Active Ingredient

OVEPOREXTON

Application Number

220860

Product Number

1

Dosage Form

-

Strength

.05MG

Approval Date

-

Regulatory Status

Unclassified

-
Unclassified Application: 220860

Drug Name

ORZEYFUL

Product Number

2

Dosage Form

-

Strength

1MG

Approval Date

-

220860 / 2

Active Ingredient

OVEPOREXTON

Application Number

220860

Product Number

2

Dosage Form

-

Strength

1MG

Approval Date

-

Regulatory Status

Unclassified

-
Unclassified Application: 220860

Drug Name

ORZEYFUL

Product Number

3

Dosage Form

-

Strength

2MG

Approval Date

-

220860 / 3

Active Ingredient

OVEPOREXTON

Application Number

220860

Product Number

3

Dosage Form

-

Strength

2MG

Approval Date

-

Regulatory Status

Unclassified

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Drug Status Breakdown
8 total
  • Unclassified
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

ENTYVIO

Application Number

125476

Product Number

1

Active Ingredient

VEDOLIZUMAB

Dosage Form

-

Strength

300MG

FDA Approved Drug Data

Approved drug product information

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Data maintained from official sources

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