CSL Vifor
FDA Approved Drugs

CSL Vifor

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 4
  • Latest Approval Date Oct 02, 2023
  • Data Source FDA
  • First Approval Date Oct 21, 2015
All
4
View
Discontinued
1
View
RX
3
View
Company Overview

Company

CSL Vifor

Country

Switzerland

Email

Social Profiles

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Company Snapshot

CSL Vifor

Flughofstrasse 61, P.O. Box CH-8152 Glattbrugg

Switzerland

www.viforpharma.com/ View on Map
FDA Approved Drug Records ( 4 records )
2015
21 Oct
RX Application: 205739

Drug Name

VELTASSA

Product Number

1

Dosage Form

-

Strength

EQ 8.4GM BASE/PACKET

Approval Date

2015-10-21

205739 / 1

Active Ingredient

PATIROMER SORBITEX CALCIUM

Application Number

205739

Product Number

1

Dosage Form

-

Strength

EQ 8.4GM BASE/PACKET

Approval Date

2015-10-21

Regulatory Status

RX

2015
21 Oct
RX Application: 205739

Drug Name

VELTASSA

Product Number

2

Dosage Form

-

Strength

EQ 16.8GM BASE/PACKET

Approval Date

2015-10-21

205739 / 2

Active Ingredient

PATIROMER SORBITEX CALCIUM

Application Number

205739

Product Number

2

Dosage Form

-

Strength

EQ 16.8GM BASE/PACKET

Approval Date

2015-10-21

Regulatory Status

RX

2015
21 Oct
Discontinued Application: 205739

Drug Name

VELTASSA

Product Number

3

Dosage Form

-

Strength

EQ 25.2GM BASE/PACKET

Approval Date

2015-10-21

205739 / 3

Active Ingredient

PATIROMER SORBITEX CALCIUM

Application Number

205739

Product Number

3

Dosage Form

-

Strength

EQ 25.2GM BASE/PACKET

Approval Date

2015-10-21

Regulatory Status

Discontinued

2023
02 Oct
RX Application: 205739

Drug Name

VELTASSA

Product Number

4

Dosage Form

-

Strength

EQ 1GM BASE/PACKET

Approval Date

2023-10-02

205739 / 4

Active Ingredient

PATIROMER SORBITEX CALCIUM

Application Number

205739

Product Number

4

Dosage Form

-

Strength

EQ 1GM BASE/PACKET

Approval Date

2023-10-02

Regulatory Status

RX

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Drug Status Breakdown
4 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

VELTASSA

Application Number

205739

Product Number

1

Active Ingredient

PATIROMER SORBITEX CALCIUM

Dosage Form

-

Strength

EQ 8.4GM BASE/PACKET

FDA Approved Drug Data

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