CPPI CV RX
FDA Approved Drugs

CPPI CV RX

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
  • Total Records 4
  • Latest Approval Date Mar 31, 2009
  • Data Source FDA
  • First Approval Date Jan 26, 2006
All
7
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Unclassified
3
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RX
4
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Company Overview

Company

CPPI CV RX

Country

Netherlands

Social Profiles

Company Snapshot

CPPI CV RX

Pfizer bvRivium Westlaan 1422909 LD Capelle a/d Ijssel

Netherlands

www.pfizer.nl/ info@pfizer.nl View on Map
FDA Approved Drug Records ( 4 records )
2006
26 Jan
RX Application: 21938

Drug Name

SUTENT

Product Number

1

Dosage Form

-

Strength

EQ 12.5MG BASE

Approval Date

2006-01-26

21938 / 1

Active Ingredient

SUNITINIB MALATE

Application Number

21938

Product Number

1

Dosage Form

-

Strength

EQ 12.5MG BASE

Approval Date

2006-01-26

Regulatory Status

RX

2006
26 Jan
RX Application: 21938

Drug Name

SUTENT

Product Number

2

Dosage Form

-

Strength

EQ 25MG BASE

Approval Date

2006-01-26

21938 / 2

Active Ingredient

SUNITINIB MALATE

Application Number

21938

Product Number

2

Dosage Form

-

Strength

EQ 25MG BASE

Approval Date

2006-01-26

Regulatory Status

RX

2006
26 Jan
RX Application: 21938

Drug Name

SUTENT

Product Number

3

Dosage Form

-

Strength

EQ 50MG BASE

Approval Date

2006-01-26

21938 / 3

Active Ingredient

SUNITINIB MALATE

Application Number

21938

Product Number

3

Dosage Form

-

Strength

EQ 50MG BASE

Approval Date

2006-01-26

Regulatory Status

RX

2009
31 Mar
RX Application: 21938

Drug Name

SUTENT

Product Number

4

Dosage Form

-

Strength

EQ 37.5MG BASE

Approval Date

2009-03-31

21938 / 4

Active Ingredient

SUNITINIB MALATE

Application Number

21938

Product Number

4

Dosage Form

-

Strength

EQ 37.5MG BASE

Approval Date

2009-03-31

Regulatory Status

RX

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Drug Status Breakdown
4 total
  • 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

SUTENT

Application Number

21938

Product Number

1

Active Ingredient

SUNITINIB MALATE

Dosage Form

-

Strength

EQ 12.5MG BASE

FDA Approved Drug Data

Approved drug product information

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