Ferring Pharmaceuticals RX
FDA Approved Drugs

Ferring Pharmaceuticals 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 7
  • Latest Approval Date Nov 28, 2017
  • Data Source FDA
  • First Approval Date Mar 30, 1995
All
42
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Unclassified
18
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Discontinued
17
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RX
7
View
Company Overview

Company

Ferring Pharmaceuticals RX

Country

Switzerland

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Company Snapshot

Ferring Pharmaceuticals RX

Ch. de la Vergognausaz 50 1162 Saint-Prex

Switzerland

www.ferring.com/ View on Map
FDA Approved Drug Records ( 7 records )
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

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

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

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

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Drug Status Breakdown
7 total
  • RX
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

CERVIDIL

Application Number

20411

Product Number

1

Active Ingredient

DINOPROSTONE

Dosage Form

-

Strength

10MG

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