Xellia Pharmaceuticals ApS Discontinued
FDA Approved Drugs

Xellia Pharmaceuticals ApS 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 7
  • Latest Approval Date Oct 18, 2019
  • Data Source FDA
  • First Approval Date Sep 09, 2015
All
15
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Discontinued
7
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RX
8
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Company Overview

Company

Xellia Pharmaceuticals ApS Discontinued

Country

Denmark

Website

Visit Website

Email

info.dk@xellia.com

Social Profiles

Company Snapshot

Xellia Pharmaceuticals ApS Discontinued

Dalslandsgade 11, 2300 Copenhagen S

Denmark

www.xellia.com/ info.dk@xellia.com View on Map
FDA Approved Drug Records ( 7 records )
2018
02 Jul
Discontinued Application: 205923

Drug Name

CASPOFUNGIN ACETATE

Product Number

1

Dosage Form

-

Strength

50MG/VIAL

Approval Date

2018-07-02

205923 / 1

Active Ingredient

CASPOFUNGIN ACETATE

Application Number

205923

Product Number

1

Dosage Form

-

Strength

50MG/VIAL

Approval Date

2018-07-02

Regulatory Status

Discontinued

2018
02 Jul
Discontinued Application: 205923

Drug Name

CASPOFUNGIN ACETATE

Product Number

2

Dosage Form

-

Strength

70MG/VIAL

Approval Date

2018-07-02

205923 / 2

Active Ingredient

CASPOFUNGIN ACETATE

Application Number

205923

Product Number

2

Dosage Form

-

Strength

70MG/VIAL

Approval Date

2018-07-02

Regulatory Status

Discontinued

2019
18 Oct
Discontinued Application: 205722

Drug Name

TIGECYCLINE

Product Number

1

Dosage Form

-

Strength

50MG/VIAL

Approval Date

2019-10-18

205722 / 1

Active Ingredient

TIGECYCLINE

Application Number

205722

Product Number

1

Dosage Form

-

Strength

50MG/VIAL

Approval Date

2019-10-18

Regulatory Status

Discontinued

2015
09 Sep
Discontinued Application: 91377

Drug Name

VANCOMYCIN HYDROCHLORIDE

Product Number

1

Dosage Form

-

Strength

EQ 500MG BASE/VIAL

Approval Date

2015-09-09

91377 / 1

Active Ingredient

VANCOMYCIN HYDROCHLORIDE

Application Number

91377

Product Number

1

Dosage Form

-

Strength

EQ 500MG BASE/VIAL

Approval Date

2015-09-09

Regulatory Status

Discontinued

2015
09 Sep
Discontinued Application: 91377

Drug Name

VANCOMYCIN HYDROCHLORIDE

Product Number

2

Dosage Form

-

Strength

EQ 1GM BASE/VIAL

Approval Date

2015-09-09

91377 / 2

Active Ingredient

VANCOMYCIN HYDROCHLORIDE

Application Number

91377

Product Number

2

Dosage Form

-

Strength

EQ 1GM BASE/VIAL

Approval Date

2015-09-09

Regulatory Status

Discontinued

2015
23 Dec
Discontinued Application: 206243

Drug Name

VANCOMYCIN HYDROCHLORIDE

Product Number

1

Dosage Form

-

Strength

EQ 5GM BASE/VIAL

Approval Date

2015-12-23

206243 / 1

Active Ingredient

VANCOMYCIN HYDROCHLORIDE

Application Number

206243

Product Number

1

Dosage Form

-

Strength

EQ 5GM BASE/VIAL

Approval Date

2015-12-23

Regulatory Status

Discontinued

2015
23 Dec
Discontinued Application: 206243

Drug Name

VANCOMYCIN HYDROCHLORIDE

Product Number

2

Dosage Form

-

Strength

EQ 10GM BASE/VIAL

Approval Date

2015-12-23

206243 / 2

Active Ingredient

VANCOMYCIN HYDROCHLORIDE

Application Number

206243

Product Number

2

Dosage Form

-

Strength

EQ 10GM BASE/VIAL

Approval Date

2015-12-23

Regulatory Status

Discontinued

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Drug Status Breakdown
7 total
  • Discontinued
Official Source

FDA approved drug data is based on publicly available U.S. Food and Drug Administration Orange Book information.

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

Drug Name

CASPOFUNGIN ACETATE

Application Number

205923

Product Number

1

Active Ingredient

CASPOFUNGIN ACETATE

Dosage Form

-

Strength

50MG/VIAL

FDA Approved Drug Data

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