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01 22care4

02 2AMW GmbH

03 11Abacus Medicine

04 26AstraZeneca

05 2Central Procurement & Supplies Unit

06 4Ebb Medical

07 2Farmagon

08 2Finno Medical Limited

09 13Medartuum

10 1Northern Medical Group Aps

11 46ORIFARM GROUP AS

12 3Oasmia Pharmaceutical

13 1Omnia L?kemedel Ab

14 1Parallel Pharma Ab

15 12Paranova Pharmaceuticals Ab

16 4Pharmachim Ab

17 5TerSera Therapeutics

18 3Teva Pharmaceutical Industries

19 2UAB Boston Biopharma LT

20 9Unimedic AB

21 2Zentiva

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PharmaCompass

01

ASPEN
Not Confirmed
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ASPEN
Not Confirmed

Goserelin Acetate

Brand Name : Zoladex

Dosage Form : Implant In Pre-Filled Syringe

Dosage Strength : 10.8mg

Packaging :

Approval Date : 06/12/2022

Application Number : 20220718000046

Regulatory Info : Approved

Registration Country : Sweden

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02

ASPEN
Not Confirmed
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ASPEN
Not Confirmed

Goserelin Acetate

Brand Name : Zoladex

Dosage Form : Implant In Pre-Filled Syringe

Dosage Strength : 10.8mg

Packaging :

Approval Date : 29/06/2016

Application Number : 20150805000058

Regulatory Info : Approved

Registration Country : Sweden

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03

ASPEN
Not Confirmed
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ASPEN
Not Confirmed

Goserelin Acetate

Brand Name : Zoladex

Dosage Form : Implant In Pre-Filled Syringe

Dosage Strength : 10.8mg

Packaging :

Approval Date : 28/02/2024

Application Number : 20231002000208

Regulatory Info : Approved

Registration Country : Sweden

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04

ASPEN
Not Confirmed
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ASPEN
Not Confirmed

Goserelin Acetate

Brand Name : Zoladex

Dosage Form : Implant In Pre-Filled Syringe

Dosage Strength : 10.8mg

Packaging :

Approval Date : 29/06/2016

Application Number : 20150805000065

Regulatory Info : Approved

Registration Country : Sweden

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05

ASPEN
Not Confirmed
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ASPEN
Not Confirmed

Goserelin

Brand Name : Zoladex

Dosage Form : Goserelin 10.8Mg 1 Unit Parenteral Use Rp

Dosage Strength : 1 syringe SC 10.8 mg prolonged release

Packaging :

Approval Date :

Application Number :

Regulatory Info :

Registration Country : Italy

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06

ASPEN
Not Confirmed
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ASPEN
Not Confirmed

Goserelin

Brand Name : Zoladex

Dosage Form : Goserelin 3,6Mg 1 Unit Parenteral Use Rp

Dosage Strength : 1 syringe SC 3.6 mg prolonged release

Packaging :

Approval Date :

Application Number :

Regulatory Info :

Registration Country : Italy

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07

ASPEN
Not Confirmed
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ASPEN
Not Confirmed

Goserelin Acetate

Brand Name : Zoladex

Dosage Form : Implant In Pre-Filled Syringe

Dosage Strength : 10.8mg

Packaging :

Approval Date : 29/03/1995

Application Number : 19950329000046

Regulatory Info : Approved

Registration Country : Sweden

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08

ASPEN
Not Confirmed
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ASPEN
Not Confirmed

Goserelin Acetate

Brand Name : Zoladex

Dosage Form : Implant In Pre-Filled Syringe

Dosage Strength : 10.8mg

Packaging :

Approval Date : 03/09/2024

Application Number : 20240513000034

Regulatory Info : Approved

Registration Country : Sweden

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09

ASPEN
Not Confirmed
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ASPEN
Not Confirmed

Goserelin Acetate

Brand Name : Zoladex

Dosage Form : Implant In Pre-Filled Syringe

Dosage Strength : 10.8mg

Packaging :

Approval Date : 20/08/2014

Application Number : 20131219000278

Regulatory Info : Approved

Registration Country : Sweden

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10

ASPEN
Not Confirmed
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ASPEN
Not Confirmed

Goserelin Acetate

Brand Name : Zoladex

Dosage Form : Implant In Pre-Filled Syringe

Dosage Strength : 10.8mg

Packaging :

Approval Date : 19/04/2007

Application Number : 20061130000067

Regulatory Info : Approved

Registration Country : Sweden

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11

ASPEN
Not Confirmed
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ASPEN
Not Confirmed

Goserelin Acetate

Brand Name : Zoladex

Dosage Form : Implant In Pre-Filled Syringe

Dosage Strength : 10.8mg

Packaging :

Approval Date : 16/10/2024

Application Number : 20240514000040

Regulatory Info : Approved

Registration Country : Sweden

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12

ASPEN
Not Confirmed
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ASPEN
Not Confirmed

Goserelin Acetate

Brand Name : Zoladex

Dosage Form : Implant In Pre-Filled Syringe

Dosage Strength : 10.8mg

Packaging :

Approval Date : 01/03/2012

Application Number : 20110331000038

Regulatory Info : Approved

Registration Country : Sweden

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13

ASPEN
Not Confirmed
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ASPEN
Not Confirmed

Goserelin Acetate

Brand Name : Zoladex

Dosage Form : Implant In Pre-Filled Syringe

Dosage Strength : 10.8mg

Packaging :

Approval Date : 20/10/2020

Application Number : 20200714000028

Regulatory Info : Approved

Registration Country : Sweden

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14

ASPEN
Not Confirmed
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ASPEN
Not Confirmed

Goserelin Acetate

Brand Name : Zoladex

Dosage Form : Implant In Pre-Filled Syringe

Dosage Strength : 10.8mg

Packaging :

Approval Date : 27/09/2012

Application Number : 20120228000089

Regulatory Info : Approved

Registration Country : Sweden

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15

ASPEN
Not Confirmed
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ASPEN
Not Confirmed

Goserelin Acetate

Brand Name : Zoladex

Dosage Form : Implant In Pre-Filled Syringe

Dosage Strength : 10.8mg

Packaging :

Approval Date : 17/04/2003

Application Number : 20030417000236

Regulatory Info : Approved

Registration Country : Sweden

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16

ASPEN
Not Confirmed
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ASPEN
Not Confirmed

Goserelin Acetate

Brand Name : Zoladex

Dosage Form : Implant In Pre-Filled Syringe

Dosage Strength : 10.8mg

Packaging :

Approval Date : 21/12/2020

Application Number : 20200909000017

Regulatory Info : Approved

Registration Country : Sweden

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17

ASPEN
Not Confirmed
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ASPEN
Not Confirmed

Goserelin Acetate

Brand Name : Zoladex

Dosage Form : Implant In Pre-Filled Syringe

Dosage Strength : 10.8mg

Packaging :

Approval Date : 13/02/2024

Application Number : 20230711000028

Regulatory Info : Approved

Registration Country : Sweden

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18

ASPEN
Not Confirmed
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ASPEN
Not Confirmed

GOSERELIN ACETATE

Brand Name : ZOLADEX

Dosage Form : IMPLANT;IMPLANTATION

Dosage Strength : EQ 3.6MG BASE

Packaging :

Approval Date : 1989-12-29

Application Number : 19726

Regulatory Info : RX

Registration Country : USA

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19

ASPEN
Not Confirmed
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ASPEN
Not Confirmed

GOSERELIN

Brand Name : ZOLADEX

Dosage Form : IMPLANT;IMPLANTATION

Dosage Strength : 3.6MG

Packaging :

Approval Date :

Application Number : 20515

Regulatory Info :

Registration Country : USA

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20

ASPEN
Not Confirmed
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ASPEN
Not Confirmed

GOSERELIN ACETATE

Brand Name : ZOLADEX

Dosage Form : IMPLANT;IMPLANTATION

Dosage Strength : EQ 10.8MG BASE

Packaging :

Approval Date : 1996-01-11

Application Number : 20578

Regulatory Info : RX

Registration Country : USA

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