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01 22care4
02 3CinnaGen Co
03 19EMD Serono
04 8Ferring Pharmaceuticals
05 5Finox Biotech AG
06 3Future Health Pharma GmbH
07 17Gedeon Richter
08 41Merck & Co
09 4Merck Group
10 7Merck Serono
11 1ORGANON CANADA
12 7ORIFARM GROUP AS
13 19Organon
14 3Teva Pharmaceutical Industries
15 9Theramex
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01 8INJ
02 2INJECTABLE;INTRAMUSCULAR, SUBCUTANEOUS
03 18INJECTABLE;SUBCUTANEOUS
04 9INJEKTIONSVÄTSKA, LÖSNING
05 4INJEKTIONSVÄTSKA, LÖSNING I CYLINDERAMPULL
06 9Inj Loose
07 3Injectable
08 1POR
09 4POWDER AND SOLVENT FOR SOLUTION FOR INJECTION
10 1POWDER FOR SOLUTION
11 1Powder and liquid for solution for injection
12 1Powder for Injection
13 10SOLUTION
14 9SOLUTION FOR INJECTION
15 3SOLUTION FOR INJECTION IN PRE-FILLED
16 5SOLUTION FOR INJECTION, PRE-FILLED SYRINGE
17 3Solution for injection
18 21Solution for injection in a pre-filled pen
19 1Trockensub
20 35Blank
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01 9Originator
02 11Prescription
03 128Blank
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01 29Bemfola
02 3Cinnal-f
03 2FOLLISTIM
04 6FOLLISTIM AQ
05 9Fertavid
06 8GONAL-F
07 3GONAL-F PEN
08 1GONAL-F RFF
09 4GONAL-F RFF REDI-JECT
10 7GONAL-f
11 6Gonal-F
12 1Gonal-F 75 I.U. (5,5µg)
13 1Gonal-F Pen 300 I.U./0.5 Ml (22µg/0.5 Ml)
14 1Gonal-F Pen 450 I.U./0.75 Ml (33µg/0.75 Ml)
15 1Gonal-F Pen 900 I.U./1.5 Ml (66µg/1.5 Ml)
16 1Gonal-f
17 9Gonal-f Pen
18 1Menopur 1 200 I.U.
19 1Menopur 600 I.U.
20 15Ovaleap
21 3PERGOVERIS
22 1PUREGON
23 1PUREGON 300 I.U/0.36 ml
24 1PUREGON 50 I.U./0,5 ml
25 1PUREGON 600 I.U./0,72 ml
26 1Pergoveris
27 3Pergoveris Pen
28 10Puregon
29 2Puregon 300 IU/0.36 mL
30 2Puregon 600 IU/0.72 mL
31 2Puregon 900 IU/1.08 mL
32 3REKOVELLE
33 6Recagon
34 3Rekovelle
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01 36Australia
02 11Canada
03 3Iran
04 25Norway
05 9South Africa
06 34Sweden
07 10Switzerland
08 20USA
Regulatory Info :
Registration Country : USA
Brand Name : GONAL-F
Dosage Form : INJECTABLE;SUBCUTANEOUS
Dosage Strength : 75 IU/VIAL
Packaging :
Approval Date :
Application Number : 20378
Regulatory Info :
Registration Country : USA
Regulatory Info :
Registration Country : USA
Brand Name : GONAL-F
Dosage Form : INJECTABLE;SUBCUTANEOUS
Dosage Strength : 150 IU/VIAL
Packaging :
Approval Date :
Application Number : 20378
Regulatory Info :
Registration Country : USA
Regulatory Info :
Registration Country : USA
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
Regulatory Info :
Registration Country : USA
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
Regulatory Info :
Registration Country : USA
Brand Name : GONAL-F
Dosage Form : INJECTABLE;SUBCUTANEOUS
Dosage Strength : 450 IU/VIAL
Packaging :
Approval Date :
Application Number : 20378
Regulatory Info :
Registration Country : USA
Regulatory Info :
Registration Country : USA
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
Regulatory Info :
Registration Country : USA
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
Regulatory Info :
Registration Country : USA
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
Regulatory Info :
Registration Country : USA
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
Regulatory Info :
Registration Country : USA
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
Regulatory Info :
Registration Country : USA
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
Regulatory Info :
Registration Country : USA
Brand Name : GONAL-F
Dosage Form : INJECTABLE;SUBCUTANEOUS
Dosage Strength : 150 IU/VIAL
Packaging :
Approval Date :
Application Number : 21765
Regulatory Info :
Registration Country : USA
Regulatory Info :
Registration Country : USA
Brand Name : FOLLISTIM
Dosage Form : INJECTABLE;INTRAMUSCULAR, SUBCUTANEOUS
Dosage Strength : 75 IU/VIAL
Packaging :
Approval Date :
Application Number : 20582
Regulatory Info :
Registration Country : USA
Regulatory Info :
Registration Country : USA
Brand Name : FOLLISTIM
Dosage Form : INJECTABLE;INTRAMUSCULAR, SUBCUTANEOUS
Dosage Strength : 150 IU/VIAL
Packaging :
Approval Date :
Application Number : 20582
Regulatory Info :
Registration Country : USA
Regulatory Info :
Registration Country : USA
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
Regulatory Info :
Registration Country : USA
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
Regulatory Info :
Registration Country : USA
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
Regulatory Info :
Registration Country : USA
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
Regulatory Info :
Registration Country : USA
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
Regulatory Info :
Registration Country : USA
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