Ferring Pharmaceuticals Unclassified
FDA Approved Drugs

Ferring Pharmaceuticals Unclassified

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
  • Total Records 18
  • Latest Approval Date -
  • Data Source FDA
  • First Approval Date -
All
42
View
Unclassified
18
View
Discontinued
17
View
RX
7
View
Company Overview

Company

Ferring Pharmaceuticals Unclassified

Country

Switzerland

Website

Visit Website

Email

Social Profiles

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Company Snapshot

Ferring Pharmaceuticals Unclassified

Ch. de la Vergognausaz 50 1162 Saint-Prex

Switzerland

www.ferring.com/ View on Map
FDA Approved Drug Records ( 18 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

-
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

-
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

-
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

-
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
18 total
  • Unclassified
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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Data maintained from official sources

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