Seagen
FDA Approved Drugs

Seagen

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 RX
  • Total Records 5
  • Latest Approval Date Apr 17, 2020
  • Data Source FDA
  • First Approval Date Apr 17, 2020
All
5
View
Unclassified
3
View
RX
2
View
Company Overview

Company

Seagen

Country

U.S.A

Social Profiles

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Company Snapshot

Seagen

21717 30th Drive S.E., Building 3 Bothell, WA 98021

U.S.A

www.seagen.com/ contact@seagen.com View on Map
FDA Approved Drug Records ( 5 records )
-
Unclassified Application: 125388

Drug Name

ADCETRIS

Product Number

1

Dosage Form

-

Strength

50MG/VIAL

Approval Date

-

125388 / 1

Active Ingredient

BRENTUXIMAB VEDOTIN

Application Number

125388

Product Number

1

Dosage Form

-

Strength

50MG/VIAL

Approval Date

-

Regulatory Status

Unclassified

-
Unclassified Application: 125399

Drug Name

ADCETRIS

Product Number

1

Dosage Form

-

Strength

50MG/VIAL

Approval Date

-

125399 / 1

Active Ingredient

BRENTUXIMAB VEDOTIN

Application Number

125399

Product Number

1

Dosage Form

-

Strength

50MG/VIAL

Approval Date

-

Regulatory Status

Unclassified

-
Unclassified Application: 761208

Drug Name

TIVDAK

Product Number

1

Dosage Form

-

Strength

40MG

Approval Date

-

761208 / 1

Active Ingredient

TISOTUMAB VEDOTIN-TFTV

Application Number

761208

Product Number

1

Dosage Form

-

Strength

40MG

Approval Date

-

Regulatory Status

Unclassified

2020
17 Apr
RX Application: 213411

Drug Name

TUKYSA

Product Number

1

Dosage Form

-

Strength

50MG

Approval Date

2020-04-17

213411 / 1

Active Ingredient

TUCATINIB

Application Number

213411

Product Number

1

Dosage Form

-

Strength

50MG

Approval Date

2020-04-17

Regulatory Status

RX

2020
17 Apr
RX Application: 213411

Drug Name

TUKYSA

Product Number

2

Dosage Form

-

Strength

150MG

Approval Date

2020-04-17

213411 / 2

Active Ingredient

TUCATINIB

Application Number

213411

Product Number

2

Dosage Form

-

Strength

150MG

Approval Date

2020-04-17

Regulatory Status

RX

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Drug Status Breakdown
5 total
  • Unclassified
  • RX
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

ADCETRIS

Application Number

125388

Product Number

1

Active Ingredient

BRENTUXIMAB VEDOTIN

Dosage Form

-

Strength

50MG/VIAL

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

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