Ferring Pharmaceuticals
FDA Approved Drugs

Ferring Pharmaceuticals

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

Company

Ferring Pharmaceuticals

Country

Switzerland

Website

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Company Snapshot

Ferring Pharmaceuticals

Ch. de la Vergognausaz 50 1162 Saint-Prex

Switzerland

www.ferring.com/ View on Map
FDA Approved Drug Records ( 42 records )
-
Unclassified Application: 17055

Drug Name

A.P.L.

Product Number

1

Dosage Form

-

Strength

5,000 UNITS/VIAL

Approval Date

-

17055 / 1

Active Ingredient

GONADOTROPIN, CHORIONIC

Application Number

17055

Product Number

1

Dosage Form

-

Strength

5,000 UNITS/VIAL

Approval Date

-

Regulatory Status

Unclassified

-
Unclassified Application: 17055

Drug Name

A.P.L.

Product Number

2

Dosage Form

-

Strength

10,000 UNITS/VIAL

Approval Date

-

17055 / 2

Active Ingredient

GONADOTROPIN, CHORIONIC

Application Number

17055

Product Number

2

Dosage Form

-

Strength

10,000 UNITS/VIAL

Approval Date

-

Regulatory Status

Unclassified

-
Unclassified Application: 17055

Drug Name

A.P.L.

Product Number

3

Dosage Form

-

Strength

20,000 UNITS/VIAL

Approval Date

-

17055 / 3

Active Ingredient

GONADOTROPIN, CHORIONIC

Application Number

17055

Product Number

3

Dosage Form

-

Strength

20,000 UNITS/VIAL

Approval Date

-

Regulatory Status

Unclassified

-
Unclassified Application: 20162

Drug Name

ACTHREL

Product Number

1

Dosage Form

-

Strength

EQ 0.1MG BASE/VIAL

Approval Date

-

20162 / 1

Active Ingredient

CORTICORELIN OVINE TRIFLUTATE

Application Number

20162

Product Number

1

Dosage Form

-

Strength

EQ 0.1MG BASE/VIAL

Approval Date

-

Regulatory Status

Unclassified

-
Unclassified Application: 19774

Drug Name

BIO-TROPIN

Product Number

1

Dosage Form

-

Strength

4.8MG/VIAL

Approval Date

-

19774 / 1

Active Ingredient

SOMATROPIN

Application Number

19774

Product Number

1

Dosage Form

-

Strength

4.8MG/VIAL

Approval Date

-

Regulatory Status

Unclassified

-
Unclassified Application: 21289

Drug Name

BRAVELLE

Product Number

1

Dosage Form

-

Strength

75 IU/VIAL

Approval Date

-

21289 / 1

Active Ingredient

UROFOLLITROPIN

Application Number

21289

Product Number

1

Dosage Form

-

Strength

75 IU/VIAL

Approval Date

-

Regulatory Status

Unclassified

-
Unclassified Application: 21484

Drug Name

BRAVELLE

Product Number

1

Dosage Form

-

Strength

0.9%

Approval Date

-

21484 / 1

Active Ingredient

UROFOLLITROPIN

Application Number

21484

Product Number

1

Dosage Form

-

Strength

0.9%

Approval Date

-

Regulatory Status

Unclassified

1995
30 Mar
RX Application: 20411

Drug Name

CERVIDIL

Product Number

1

Dosage Form

-

Strength

10MG

Approval Date

1995-03-30

20411 / 1

Active Ingredient

DINOPROSTONE

Application Number

20411

Product Number

1

Dosage Form

-

Strength

10MG

Approval Date

1995-03-30

Regulatory Status

RX

-
Unclassified Application: 17016

Drug Name

CHORIONIC GONADOTROPIN

Product Number

4

Dosage Form

-

Strength

20,000 UNITS/VIAL

Approval Date

-

17016 / 4

Active Ingredient

GONADOTROPIN, CHORIONIC

Application Number

17016

Product Number

4

Dosage Form

-

Strength

20,000 UNITS/VIAL

Approval Date

-

Regulatory Status

Unclassified

-
Unclassified Application: 17016

Drug Name

CHORIONIC GONADOTROPIN

Product Number

6

Dosage Form

-

Strength

5,000 UNITS/VIAL

Approval Date

-

17016 / 6

Active Ingredient

GONADOTROPIN, CHORIONIC

Application Number

17016

Product Number

6

Dosage Form

-

Strength

5,000 UNITS/VIAL

Approval Date

-

Regulatory Status

Unclassified

-
Unclassified Application: 17016

Drug Name

CHORIONIC GONADOTROPIN

Product Number

7

Dosage Form

-

Strength

10,000 UNITS/VIAL

Approval Date

-

17016 / 7

Active Ingredient

GONADOTROPIN, CHORIONIC

Application Number

17016

Product Number

7

Dosage Form

-

Strength

10,000 UNITS/VIAL

Approval Date

-

Regulatory Status

Unclassified

-
Unclassified Application: 17016

Drug Name

CHORIONIC GONADOTROPIN

Product Number

9

Dosage Form

-

Strength

2,000 UNITS/VIAL

Approval Date

-

17016 / 9

Active Ingredient

GONADOTROPIN, CHORIONIC

Application Number

17016

Product Number

9

Dosage Form

-

Strength

2,000 UNITS/VIAL

Approval Date

-

Regulatory Status

Unclassified

-
Unclassified Application: 17016

Drug Name

CHORIONIC GONADOTROPIN

Product Number

10

Dosage Form

-

Strength

15,000 UNITS/VIAL

Approval Date

-

17016 / 10

Active Ingredient

GONADOTROPIN, CHORIONIC

Application Number

17016

Product Number

10

Dosage Form

-

Strength

15,000 UNITS/VIAL

Approval Date

-

Regulatory Status

Unclassified

-
Unclassified Application: 17016

Drug Name

CHORIONIC GONADOTROPIN

Product Number

11

Dosage Form

-

Strength

2,000 UNITS/VIAL

Approval Date

-

17016 / 11

Active Ingredient

GONADOTROPIN, CHORIONIC

Application Number

17016

Product Number

11

Dosage Form

-

Strength

2,000 UNITS/VIAL

Approval Date

-

Regulatory Status

Unclassified

2017
28 Nov
RX Application: 209589

Drug Name

CLENPIQ

Product Number

1

Dosage Form

-

Strength

12GM/BOT;3.5GM/BOT;10MG/BOT

Approval Date

2017-11-28

209589 / 1

Active Ingredient

CITRIC ACID; MAGNESIUM OXIDE; SODIUM PICOSULFATE

Application Number

209589

Product Number

1

Dosage Form

-

Strength

12GM/BOT;3.5GM/BOT;10MG/BOT

Approval Date

2017-11-28

Regulatory Status

RX

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

1995
06 Sep
RX Application: 19955

Drug Name

DDAVP

Product Number

1

Dosage Form

-

Strength

0.1MG

Approval Date

1995-09-06

19955 / 1

Active Ingredient

DESMOPRESSIN ACETATE

Application Number

19955

Product Number

1

Dosage Form

-

Strength

0.1MG

Approval Date

1995-09-06

Regulatory Status

RX

1995
06 Sep
RX Application: 19955

Drug Name

DDAVP

Product Number

2

Dosage Form

-

Strength

0.2MG

Approval Date

1995-09-06

19955 / 2

Active Ingredient

DESMOPRESSIN ACETATE

Application Number

19955

Product Number

2

Dosage Form

-

Strength

0.2MG

Approval Date

1995-09-06

Regulatory Status

RX

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

2007
21 Jun
RX Application: 22057

Drug Name

ENDOMETRIN

Product Number

1

Dosage Form

-

Strength

100MG

Approval Date

2007-06-21

22057 / 1

Active Ingredient

PROGESTERONE

Application Number

22057

Product Number

1

Dosage Form

-

Strength

100MG

Approval Date

2007-06-21

Regulatory Status

RX

2008
24 Dec
RX Application: 22201

Drug Name

FIRMAGON

Product Number

1

Dosage Form

-

Strength

EQ 80MG BASE/VIAL

Approval Date

2008-12-24

22201 / 1

Active Ingredient

DEGARELIX ACETATE

Application Number

22201

Product Number

1

Dosage Form

-

Strength

EQ 80MG BASE/VIAL

Approval Date

2008-12-24

Regulatory Status

RX

2008
24 Dec
RX Application: 22201

Drug Name

FIRMAGON

Product Number

2

Dosage Form

-

Strength

EQ 120MG BASE/VIAL

Approval Date

2008-12-24

22201 / 2

Active Ingredient

DEGARELIX ACETATE

Application Number

22201

Product Number

2

Dosage Form

-

Strength

EQ 120MG BASE/VIAL

Approval Date

2008-12-24

Regulatory Status

RX

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

-
Unclassified Application: 21663

Drug Name

MENOPUR

Product Number

1

Dosage Form

-

Strength

75 IU/VIAL;75 IU/VIAL

Approval Date

-

21663 / 1

Active Ingredient

MENOTROPINS (FSH;LH)

Application Number

21663

Product Number

1

Dosage Form

-

Strength

75 IU/VIAL;75 IU/VIAL

Approval Date

-

Regulatory Status

Unclassified

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

-
Unclassified Application: 21047

Drug Name

REPRONEX

Product Number

1

Dosage Form

-

Strength

75 IU/VIAL;75 IU/VIAL

Approval Date

-

21047 / 1

Active Ingredient

MENOTROPINS (FSH;LH)

Application Number

21047

Product Number

1

Dosage Form

-

Strength

75 IU/VIAL;75 IU/VIAL

Approval Date

-

Regulatory Status

Unclassified

-
Unclassified Application: 21047

Drug Name

REPRONEX

Product Number

2

Dosage Form

-

Strength

150 IU/VIAL;150 IU/VIAL

Approval Date

-

21047 / 2

Active Ingredient

MENOTROPINS (FSH;LH)

Application Number

21047

Product Number

2

Dosage Form

-

Strength

150 IU/VIAL;150 IU/VIAL

Approval Date

-

Regulatory Status

Unclassified

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

-
Unclassified Application: 19774

Drug Name

ZOMACTON

Product Number

2

Dosage Form

-

Strength

5MG/VIAL

Approval Date

-

19774 / 2

Active Ingredient

SOMATROPIN

Application Number

19774

Product Number

2

Dosage Form

-

Strength

5MG/VIAL

Approval Date

-

Regulatory Status

Unclassified

-
Unclassified Application: 19774

Drug Name

ZOMACTON

Product Number

3

Dosage Form

-

Strength

10MG/VIAL

Approval Date

-

19774 / 3

Active Ingredient

SOMATROPIN

Application Number

19774

Product Number

3

Dosage Form

-

Strength

10MG/VIAL

Approval Date

-

Regulatory Status

Unclassified

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Drug Status Breakdown
42 total
  • Unclassified
  • 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

A.P.L.

Application Number

17055

Product Number

1

Active Ingredient

GONADOTROPIN, CHORIONIC

Dosage Form

-

Strength

5,000 UNITS/VIAL

FDA Approved Drug Data

Approved drug product information

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