Ferring Pharmaceuticals Discontinued
FDA Approved Drugs

Ferring Pharmaceuticals 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 17
  • Latest Approval Date Apr 29, 2020
  • Data Source FDA
  • First Approval Date Jan 01, 1982
All
42
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Unclassified
18
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Discontinued
17
View
RX
7
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Company Overview

Company

Ferring Pharmaceuticals Discontinued

Country

Switzerland

Website

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Company Snapshot

Ferring Pharmaceuticals Discontinued

Ch. de la Vergognausaz 50 1162 Saint-Prex

Switzerland

www.ferring.com/ View on Map
FDA Approved Drug Records ( 17 records )
1990
26 Dec
Discontinued Application: 19776

Drug Name

CONCENTRAID

Product Number

1

Dosage Form

-

Strength

0.01%

Approval Date

1990-12-26

19776 / 1

Active Ingredient

DESMOPRESSIN ACETATE

Application Number

19776

Product Number

1

Dosage Form

-

Strength

0.01%

Approval Date

1990-12-26

Regulatory Status

Discontinued

1982
01 Jan
Discontinued Application: 17922

Drug Name

DDAVP

Product Number

1

Dosage Form

-

Strength

0.01%

Approval Date

1982-01-01

17922 / 1

Active Ingredient

DESMOPRESSIN ACETATE

Application Number

17922

Product Number

1

Dosage Form

-

Strength

0.01%

Approval Date

1982-01-01

Regulatory Status

Discontinued

1989
06 Feb
Discontinued Application: 17922

Drug Name

DDAVP

Product Number

2

Dosage Form

-

Strength

0.01MG/SPRAY **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons**

Approval Date

1989-02-06

17922 / 2

Active Ingredient

DESMOPRESSIN ACETATE

Application Number

17922

Product Number

2

Dosage Form

-

Strength

0.01MG/SPRAY **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons**

Approval Date

1989-02-06

Regulatory Status

Discontinued

1996
07 Aug
Discontinued Application: 17922

Drug Name

DDAVP (NEEDS NO REFRIGERATION)

Product Number

3

Dosage Form

-

Strength

0.01MG/SPRAY

Approval Date

1996-08-07

17922 / 3

Active Ingredient

DESMOPRESSIN ACETATE

Application Number

17922

Product Number

3

Dosage Form

-

Strength

0.01MG/SPRAY

Approval Date

1996-08-07

Regulatory Status

Discontinued

2008
08 May
Discontinued Application: 21795

Drug Name

DESMOPRESSIN ACETATE

Product Number

1

Dosage Form

-

Strength

0.1MG

Approval Date

2008-05-08

21795 / 1

Active Ingredient

DESMOPRESSIN ACETATE

Application Number

21795

Product Number

1

Dosage Form

-

Strength

0.1MG

Approval Date

2008-05-08

Regulatory Status

Discontinued

2008
08 May
Discontinued Application: 21795

Drug Name

DESMOPRESSIN ACETATE

Product Number

2

Dosage Form

-

Strength

0.2MG

Approval Date

2008-05-08

21795 / 2

Active Ingredient

DESMOPRESSIN ACETATE

Application Number

21795

Product Number

2

Dosage Form

-

Strength

0.2MG

Approval Date

2008-05-08

Regulatory Status

Discontinued

1989
10 Oct
Discontinued Application: 19687

Drug Name

LUTREPULSE KIT

Product Number

1

Dosage Form

-

Strength

0.8MG/VIAL

Approval Date

1989-10-10

19687 / 1

Active Ingredient

GONADORELIN ACETATE

Application Number

19687

Product Number

1

Dosage Form

-

Strength

0.8MG/VIAL

Approval Date

1989-10-10

Regulatory Status

Discontinued

1989
10 Oct
Discontinued Application: 19687

Drug Name

LUTREPULSE KIT

Product Number

2

Dosage Form

-

Strength

3.2MG/VIAL

Approval Date

1989-10-10

19687 / 2

Active Ingredient

GONADORELIN ACETATE

Application Number

19687

Product Number

2

Dosage Form

-

Strength

3.2MG/VIAL

Approval Date

1989-10-10

Regulatory Status

Discontinued

2020
29 Apr
Discontinued Application: 201110

Drug Name

MILPROSA

Product Number

1

Dosage Form

-

Strength

1.78GM

Approval Date

2020-04-29

201110 / 1

Active Ingredient

PROGESTERONE

Application Number

201110

Product Number

1

Dosage Form

-

Strength

1.78GM

Approval Date

2020-04-29

Regulatory Status

Discontinued

2002
16 Sep
Discontinued Application: 21333

Drug Name

MINIRIN

Product Number

1

Dosage Form

-

Strength

0.01MG/SPRAY

Approval Date

2002-09-16

21333 / 1

Active Ingredient

DESMOPRESSIN ACETATE

Application Number

21333

Product Number

1

Dosage Form

-

Strength

0.01MG/SPRAY

Approval Date

2002-09-16

Regulatory Status

Discontinued

2018
21 Jun
Discontinued Application: 22517

Drug Name

NOCDURNA

Product Number

1

Dosage Form

-

Strength

0.0277MG

Approval Date

2018-06-21

22517 / 1

Active Ingredient

DESMOPRESSIN ACETATE

Application Number

22517

Product Number

1

Dosage Form

-

Strength

0.0277MG

Approval Date

2018-06-21

Regulatory Status

Discontinued

2018
21 Jun
Discontinued Application: 22517

Drug Name

NOCDURNA

Product Number

2

Dosage Form

-

Strength

0.0553MG

Approval Date

2018-06-21

22517 / 2

Active Ingredient

DESMOPRESSIN ACETATE

Application Number

22517

Product Number

2

Dosage Form

-

Strength

0.0553MG

Approval Date

2018-06-21

Regulatory Status

Discontinued

2012
16 Jul
Discontinued Application: 202535

Drug Name

PREPOPIK

Product Number

1

Dosage Form

-

Strength

12GM/PACKET;3.5GM/PACKET;10MG/PACKET **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons**

Approval Date

2012-07-16

202535 / 1

Active Ingredient

CITRIC ACID; MAGNESIUM OXIDE; SODIUM PICOSULFATE

Application Number

202535

Product Number

1

Dosage Form

-

Strength

12GM/PACKET;3.5GM/PACKET;10MG/PACKET **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons**

Approval Date

2012-07-16

Regulatory Status

Discontinued

1982
01 Jan
Discontinued Application: 18290

Drug Name

SECRETIN-FERRING

Product Number

1

Dosage Form

-

Strength

75CU/VIAL

Approval Date

1982-01-01

18290 / 1

Active Ingredient

SECRETIN

Application Number

18290

Product Number

1

Dosage Form

-

Strength

75CU/VIAL

Approval Date

1982-01-01

Regulatory Status

Discontinued

1994
07 Mar
Discontinued Application: 20355

Drug Name

STIMATE

Product Number

1

Dosage Form

-

Strength

0.15MG/SPRAY

Approval Date

1994-03-07

20355 / 1

Active Ingredient

DESMOPRESSIN ACETATE

Application Number

20355

Product Number

1

Dosage Form

-

Strength

0.15MG/SPRAY

Approval Date

1994-03-07

Regulatory Status

Discontinued

2007
24 Oct
Discontinued Application: 20355

Drug Name

STIMATE (NEEDS NO REFRIGERATION)

Product Number

2

Dosage Form

-

Strength

0.15MG/SPRAY

Approval Date

2007-10-24

20355 / 2

Active Ingredient

DESMOPRESSIN ACETATE

Application Number

20355

Product Number

2

Dosage Form

-

Strength

0.15MG/SPRAY

Approval Date

2007-10-24

Regulatory Status

Discontinued

1982
01 Jan
Discontinued Application: 18087

Drug Name

THYREL TRH

Product Number

1

Dosage Form

-

Strength

0.5MG/ML

Approval Date

1982-01-01

18087 / 1

Active Ingredient

PROTIRELIN

Application Number

18087

Product Number

1

Dosage Form

-

Strength

0.5MG/ML

Approval Date

1982-01-01

Regulatory Status

Discontinued

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Drug Status Breakdown
17 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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FDA Approved Drug Record Details Preview

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

Drug Name

CONCENTRAID

Application Number

19776

Product Number

1

Active Ingredient

DESMOPRESSIN ACETATE

Dosage Form

-

Strength

0.01%

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