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01 22care4

02 3CinnaGen

03 19EMD Serono

04 21Ferring Pharmaceuticals

05 34Gedeon Richter

06 3Labatec Pharm

07 55Merck & Co

08 19Merck Group

09 4Merck Serono

10 1ORGANON CANADA INC.

11 7ORIFARM GROUP AS

12 26Organon

13 3Organon South Africa (Pty) Ltd

14 15Theramex

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PharmaCompass

01

Fall Technical Meeting
Not Confirmed
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Fall Technical Meeting
Not Confirmed

FOLLITROPIN ALFA/BETA

Brand Name : GONAL-F

Dosage Form : INJECTABLE;SUBCUTANEOUS

Dosage Strength : 75 IU/VIAL

Packaging :

Approval Date :

Application Number : 20378

Regulatory Info :

Registration Country : USA

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02

Fall Technical Meeting
Not Confirmed
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arrow
Fall Technical Meeting
Not Confirmed

FOLLITROPIN ALFA/BETA

Brand Name : GONAL-F

Dosage Form : INJECTABLE;SUBCUTANEOUS

Dosage Strength : 150 IU/VIAL

Packaging :

Approval Date :

Application Number : 20378

Regulatory Info :

Registration Country : USA

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03

Fall Technical Meeting
Not Confirmed
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Fall Technical Meeting
Not Confirmed

FOLLITROPIN ALFA/BETA

Brand Name : GONAL-F

Dosage Form : INJECTABLE;SUBCUTANEOUS

Dosage Strength : 37.5 IU/VIAL

Packaging :

Approval Date :

Application Number : 20378

Regulatory Info :

Registration Country : USA

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04

Fall Technical Meeting
Not Confirmed
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Fall Technical Meeting
Not Confirmed

FOLLITROPIN ALFA/BETA

Brand Name : GONAL-F

Dosage Form : INJECTABLE;SUBCUTANEOUS

Dosage Strength : 1,050 IU/VIAL

Packaging :

Approval Date :

Application Number : 20378

Regulatory Info :

Registration Country : USA

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05

Fall Technical Meeting
Not Confirmed
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arrow
Fall Technical Meeting
Not Confirmed

FOLLITROPIN ALFA/BETA

Brand Name : GONAL-F

Dosage Form : INJECTABLE;SUBCUTANEOUS

Dosage Strength : 450 IU/VIAL

Packaging :

Approval Date :

Application Number : 20378

Regulatory Info :

Registration Country : USA

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06

Fall Technical Meeting
Not Confirmed
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Fall Technical Meeting
Not Confirmed

FOLLITROPIN ALFA/BETA

Brand Name : GONAL-F RFF REDI-JECT

Dosage Form : INJECTABLE;SUBCUTANEOUS

Dosage Strength : 300 IU/0.5ML

Packaging :

Approval Date :

Application Number : 21684

Regulatory Info :

Registration Country : USA

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07

Fall Technical Meeting
Not Confirmed
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Fall Technical Meeting
Not Confirmed

FOLLITROPIN ALFA/BETA

Brand Name : GONAL-F RFF REDI-JECT

Dosage Form : INJECTABLE;SUBCUTANEOUS

Dosage Strength : 450 IU/0.75ML

Packaging :

Approval Date :

Application Number : 21684

Regulatory Info :

Registration Country : USA

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08

Fall Technical Meeting
Not Confirmed
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Fall Technical Meeting
Not Confirmed

FOLLITROPIN ALFA/BETA

Brand Name : GONAL-F RFF REDI-JECT

Dosage Form : INJECTABLE;SUBCUTANEOUS

Dosage Strength : 900 IU/1.5ML

Packaging :

Approval Date :

Application Number : 21684

Regulatory Info :

Registration Country : USA

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09

Fall Technical Meeting
Not Confirmed
arrow
arrow
Fall Technical Meeting
Not Confirmed

FOLLITROPIN ALFA/BETA

Brand Name : GONAL-F RFF REDI-JECT

Dosage Form : INJECTABLE;SUBCUTANEOUS

Dosage Strength : 150 IU/0.25ML

Packaging :

Approval Date :

Application Number : 21684

Regulatory Info :

Registration Country : USA

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10

Fall Technical Meeting
Not Confirmed
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arrow
Fall Technical Meeting
Not Confirmed

FOLLITROPIN ALFA/BETA

Brand Name : GONAL-F

Dosage Form : INJECTABLE;SUBCUTANEOUS

Dosage Strength : 37.5 IU/VIAL

Packaging :

Approval Date :

Application Number : 21765

Regulatory Info :

Registration Country : USA

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11

Fall Technical Meeting
Not Confirmed
arrow
arrow
Fall Technical Meeting
Not Confirmed

FOLLITROPIN ALFA/BETA

Brand Name : GONAL-F RFF

Dosage Form : INJECTABLE;SUBCUTANEOUS

Dosage Strength : 75 IU/VIAL

Packaging :

Approval Date :

Application Number : 21765

Regulatory Info :

Registration Country : USA

blank

12

Fall Technical Meeting
Not Confirmed
arrow
arrow
Fall Technical Meeting
Not Confirmed

FOLLITROPIN ALFA/BETA

Brand Name : GONAL-F

Dosage Form : INJECTABLE;SUBCUTANEOUS

Dosage Strength : 150 IU/VIAL

Packaging :

Approval Date :

Application Number : 21765

Regulatory Info :

Registration Country : USA

blank

13

Fall Technical Meeting
Not Confirmed
arrow
arrow
Fall Technical Meeting
Not Confirmed

FOLLITROPIN ALFA/BETA

Brand Name : FOLLISTIM

Dosage Form : INJECTABLE;INTRAMUSCULAR, SUBCUTANEOUS

Dosage Strength : 75 IU/VIAL

Packaging :

Approval Date :

Application Number : 20582

Regulatory Info :

Registration Country : USA

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14

Fall Technical Meeting
Not Confirmed
arrow
arrow
Fall Technical Meeting
Not Confirmed

FOLLITROPIN ALFA/BETA

Brand Name : FOLLISTIM

Dosage Form : INJECTABLE;INTRAMUSCULAR, SUBCUTANEOUS

Dosage Strength : 150 IU/VIAL

Packaging :

Approval Date :

Application Number : 20582

Regulatory Info :

Registration Country : USA

blank

15

Fall Technical Meeting
Not Confirmed
arrow
arrow
Fall Technical Meeting
Not Confirmed

FOLLITROPIN ALFA/BETA

Brand Name : FOLLISTIM AQ

Dosage Form : INJECTABLE;SUBCUTANEOUS

Dosage Strength : 75 IU/0.5ML

Packaging :

Approval Date :

Application Number : 21273

Regulatory Info :

Registration Country : USA

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16

Fall Technical Meeting
Not Confirmed
arrow
arrow
Fall Technical Meeting
Not Confirmed

FOLLITROPIN ALFA/BETA

Brand Name : FOLLISTIM AQ

Dosage Form : INJECTABLE;SUBCUTANEOUS

Dosage Strength : 150 IU/0.5ML

Packaging :

Approval Date :

Application Number : 21273

Regulatory Info :

Registration Country : USA

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17

Fall Technical Meeting
Not Confirmed
arrow
arrow
Fall Technical Meeting
Not Confirmed

FOLLITROPIN ALFA/BETA

Brand Name : FOLLISTIM AQ

Dosage Form : INJECTABLE;SUBCUTANEOUS

Dosage Strength : 300 IU/0.36ML

Packaging :

Approval Date :

Application Number : 21211

Regulatory Info :

Registration Country : USA

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18

Fall Technical Meeting
Not Confirmed
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Fall Technical Meeting
Not Confirmed

FOLLITROPIN ALFA/BETA

Brand Name : FOLLISTIM AQ

Dosage Form : INJECTABLE;SUBCUTANEOUS

Dosage Strength : 600 IU/0.72ML

Packaging :

Approval Date :

Application Number : 21211

Regulatory Info :

Registration Country : USA

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19

Fall Technical Meeting
Not Confirmed
arrow
arrow
Fall Technical Meeting
Not Confirmed

FOLLITROPIN ALFA/BETA

Brand Name : FOLLISTIM AQ

Dosage Form : INJECTABLE;SUBCUTANEOUS

Dosage Strength : 150 IU/0.18ML

Packaging :

Approval Date :

Application Number : 21211

Regulatory Info :

Registration Country : USA

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20

Fall Technical Meeting
Not Confirmed
arrow
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Fall Technical Meeting
Not Confirmed

FOLLITROPIN ALFA/BETA

Brand Name : FOLLISTIM AQ

Dosage Form : INJECTABLE;SUBCUTANEOUS

Dosage Strength : 900 IU/1.08ML

Packaging :

Approval Date :

Application Number : 21211

Regulatory Info :

Registration Country : USA

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