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01 2Ferring Pharmaceuticals

02 6IBSA Institut Biochimique

03 8Ibsa Biochemical Institute Sa

04 5Merck & Co

05 2ORIFARM GROUP AS

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PharmaCompass

01

FNCE
Not Confirmed
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FNCE
Not Confirmed

Urofollitropin

Brand Name : Bravelle

Dosage Form : Solution For Injection

Dosage Strength : 75IE

Packaging :

Approval Date : 07/04/2006

Application Number : 20050520000015

Regulatory Info : Deregistered

Registration Country : Sweden

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02

FNCE
Not Confirmed
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FNCE
Not Confirmed

Urofollitropin

Brand Name : Fostimon

Dosage Form : Solution For Injection

Dosage Strength : 150IE

Packaging :

Approval Date : 05/07/2007

Application Number : 20050929000029

Regulatory Info : Approved

Registration Country : Sweden

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03

FNCE
Not Confirmed
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FNCE
Not Confirmed

Urofollitropin

Brand Name : Fostimon

Dosage Form : Solution For Injection

Dosage Strength : 75IE

Packaging :

Approval Date : 05/07/2007

Application Number : 20050929000012

Regulatory Info : Approved

Registration Country : Sweden

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04

FNCE
Not Confirmed
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FNCE
Not Confirmed

Urofollitropin

Brand Name : Fostimon Set

Dosage Form : Solution For Injection

Dosage Strength : 150IE

Packaging :

Approval Date : 26/10/2012

Application Number : 20110617000028

Regulatory Info : Approved

Registration Country : Sweden

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05

FNCE
Not Confirmed
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FNCE
Not Confirmed

Urofollitropin

Brand Name : Fostimon Set

Dosage Form : Solution For Injection

Dosage Strength : 225IE

Packaging :

Approval Date : 14/02/2013

Application Number : 20120222000030

Regulatory Info : Approved

Registration Country : Sweden

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06

FNCE
Not Confirmed
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FNCE
Not Confirmed

Urofollitropin

Brand Name : Fostimon Set

Dosage Form : Solution For Injection

Dosage Strength : 300IE

Packaging :

Approval Date : 14/02/2013

Application Number : 20120222000047

Regulatory Info : Approved

Registration Country : Sweden

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07

FNCE
Not Confirmed
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FNCE
Not Confirmed

Urofollitropin

Brand Name : Fostimon Set

Dosage Form : Solution For Injection

Dosage Strength : 75IE

Packaging :

Approval Date : 26/10/2012

Application Number : 20110617000011

Regulatory Info : Approved

Registration Country : Sweden

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08

FNCE
Not Confirmed
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FNCE
Not Confirmed

Follistim

Brand Name : Puregon

Dosage Form : Follitropin Beta 100Iu 0,5Ml 5 Units Parenteral Use

Dosage Strength : 5 VIALS IM SC 100 IU 0.5 ml

Packaging :

Approval Date :

Application Number :

Regulatory Info :

Registration Country : Italy

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09

FNCE
Not Confirmed
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FNCE
Not Confirmed

Follistim

Brand Name : Puregon

Dosage Form : Follitropin Beta 300Iu 0.36Ml 1 Units Parenteral Use

Dosage Strength : 1 cartridge SC 300 IU/0.36 ml

Packaging :

Approval Date :

Application Number :

Regulatory Info :

Registration Country : Italy

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10

FNCE
Not Confirmed
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FNCE
Not Confirmed

Follistim

Brand Name : Puregon

Dosage Form : Follitropin Beta 50Iu 0,5Ml 5 Units Parenteral Use

Dosage Strength : 5 VIALS IM SC 50 IU 0.5 ml

Packaging :

Approval Date :

Application Number :

Regulatory Info :

Registration Country : Italy

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11

FNCE
Not Confirmed
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FNCE
Not Confirmed

Follistim

Brand Name : Puregon

Dosage Form : Follitropin Beta 600Iu 0.72Ml 1 Units Parenteral Use

Dosage Strength : 1 cartridge SC 600 IU/0.72 ml

Packaging :

Approval Date :

Application Number :

Regulatory Info :

Registration Country : Italy

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12

FNCE
Not Confirmed
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FNCE
Not Confirmed

Follistim

Brand Name : Puregon

Dosage Form : Follitropin Beta 900Iu 1.08 Ml 1 Units Parenteral Use

Dosage Strength : 1 cartridge SC 900 IU/1.08 ml

Packaging :

Approval Date :

Application Number :

Regulatory Info :

Registration Country : Italy

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13

FNCE
Not Confirmed
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FNCE
Not Confirmed

Urofollitropin

Brand Name : Fostimon Set

Dosage Form : Solution For Injection

Dosage Strength : 150IE

Packaging :

Approval Date : 03/02/2016

Application Number : 20140801000046

Regulatory Info : Deregistered

Registration Country : Sweden

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14

FNCE
Not Confirmed
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FNCE
Not Confirmed

Urofollitropin

Brand Name : Fostimon Set

Dosage Form : Solution For Injection

Dosage Strength : 150IE

Packaging :

Approval Date : 04/06/2019

Application Number : 20190220000073

Regulatory Info : Deregistered

Registration Country : Sweden

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15

Ibsa Biochemical Institute Sa

Country
FNCE
Not Confirmed
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Ibsa Biochemical Institute Sa

Country
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FNCE
Not Confirmed

Urofollitropin

Brand Name : Fostimon UI

Dosage Form : Injectable Solution

Dosage Strength : 75IU/ml

Packaging :

Approval Date : 18/07/1996

Application Number : 52974

Regulatory Info : Allowed

Registration Country : Switzerland

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16

Ibsa Biochemical Institute Sa

Country
FNCE
Not Confirmed
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Ibsa Biochemical Institute Sa

Country
arrow
FNCE
Not Confirmed

Urofollitropin

Brand Name : Fostimon UI

Dosage Form : Injectable Solution

Dosage Strength : 150IU/ml

Packaging :

Approval Date : 18/07/1996

Application Number : 52974

Regulatory Info : Allowed

Registration Country : Switzerland

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17

Ibsa Biochemical Institute Sa

Country
FNCE
Not Confirmed
arrow

Ibsa Biochemical Institute Sa

Country
arrow
FNCE
Not Confirmed

Urofollitropin

Brand Name : Fostimon UI

Dosage Form : Injectable Solution

Dosage Strength : 75IU/ml

Packaging :

Approval Date : 18/07/1996

Application Number : 52974

Regulatory Info : Allowed

Registration Country : Switzerland

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18

Ibsa Biochemical Institute Sa

Country
FNCE
Not Confirmed
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Ibsa Biochemical Institute Sa

Country
arrow
FNCE
Not Confirmed

Urofollitropin

Brand Name : Fostimon UI

Dosage Form : Injectable Solution

Dosage Strength : 150IU/ml

Packaging :

Approval Date : 18/07/1996

Application Number : 52974

Regulatory Info : Allowed

Registration Country : Switzerland

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19

Ibsa Biochemical Institute Sa

Country
FNCE
Not Confirmed
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Ibsa Biochemical Institute Sa

Country
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FNCE
Not Confirmed

Urofollitropin

Brand Name : Fostimon UI

Dosage Form : Injectable Solution

Dosage Strength : 225IU/ml

Packaging :

Approval Date : 18/07/1996

Application Number : 52974

Regulatory Info : Allowed

Registration Country : Switzerland

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20

Ibsa Biochemical Institute Sa

Country
FNCE
Not Confirmed
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Ibsa Biochemical Institute Sa

Country
arrow
FNCE
Not Confirmed

Urofollitropin

Brand Name : Fostimon UI

Dosage Form : Injectable Solution

Dosage Strength : 300IU/ml

Packaging :

Approval Date : 18/07/1996

Application Number : 52974

Regulatory Info : Allowed

Registration Country : Switzerland

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