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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

ASCO GU
Not Confirmed
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ASCO GU
Not Confirmed

Goserelin

Brand Name : Golexin La

Dosage Form : Implant

Dosage Strength : 10.8MG

Packaging :

Approval Date : 2016-08-26

Application Number :

Regulatory Info : Authorised

Registration Country : Malta

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02

ASCO GU
Not Confirmed
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ASCO GU
Not Confirmed

Goserelin

Brand Name : Golexin In A Pre-Filled Syringe Implants

Dosage Form : Implant

Dosage Strength : 3.6MG

Packaging :

Approval Date : 2016-08-26

Application Number :

Regulatory Info : Authorised

Registration Country : Malta

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03

ASCO GU
Not Confirmed
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ASCO GU
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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04

ASCO GU
Not Confirmed
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ASCO GU
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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05

ASCO GU
Not Confirmed
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ASCO GU
Not Confirmed

Goserelinum

Brand Name : Zoladex SafeSystem

Dosage Form : Injectable Solution

Dosage Strength : 3.6mg

Packaging :

Approval Date : 28/06/1990

Application Number : 48159

Regulatory Info : Allowed

Registration Country : Switzerland

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06

ASCO GU
Not Confirmed
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ASCO GU
Not Confirmed

Goserelinum

Brand Name : Zoladex LA SafeSystem

Dosage Form : Injectable Solution

Dosage Strength : 10.8mg

Packaging :

Approval Date : 27/12/1995

Application Number : 53371

Regulatory Info : Allowed

Registration Country : Switzerland

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07

ASCO GU
Not Confirmed
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ASCO GU
Not Confirmed

Goserelin

Brand Name : Zoladex

Dosage Form : Implant

Dosage Strength : 3.6MG

Packaging :

Approval Date : 2005-10-31

Application Number :

Regulatory Info : Authorised

Registration Country : Malta

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08

ASCO GU
Not Confirmed
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ASCO GU
Not Confirmed

Goserelin

Brand Name : Zoladex La

Dosage Form : Implant

Dosage Strength : 10.8MG

Packaging :

Approval Date : 2005-10-31

Application Number :

Regulatory Info : Authorised

Registration Country : Malta

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09

ASCO GU
Not Confirmed
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ASCO GU
Not Confirmed

Goserelin

Brand Name : Zoladex

Dosage Form : Implant

Dosage Strength : 3.6mg

Packaging :

Approval Date : 27-12-2021

Application Number :

Regulatory Info :

Registration Country : Moldova

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10

ASCO GU
Not Confirmed
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ASCO GU
Not Confirmed

Goserelin

Brand Name : Zoladex LA

Dosage Form : Implant

Dosage Strength : 10.8mg

Packaging :

Approval Date : 27-12-2021

Application Number :

Regulatory Info :

Registration Country : Moldova

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11

ASCO GU
Not Confirmed
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ASCO GU
Not Confirmed

Goserelin acetate

Brand Name : Zoladex

Dosage Form : Implant

Dosage Strength : 10.8mg

Packaging :

Approval Date :

Application Number :

Regulatory Info : Marketed

Registration Country : Norway

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12

ASCO GU
Not Confirmed
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ASCO GU
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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13

ASCO GU
Not Confirmed
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ASCO GU
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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14

ASCO GU
Not Confirmed
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ASCO GU
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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15

Central Procurement & Supplies Unit

Country
ASCO GU
Not Confirmed
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Central Procurement & Supplies Unit

Country
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ASCO GU
Not Confirmed

Goserelin

Brand Name : Zoladex La

Dosage Form : Implant

Dosage Strength : 10.8MG

Packaging :

Approval Date : 2020-06-08

Application Number :

Regulatory Info : Invalid

Registration Country : Malta

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16

Central Procurement & Supplies Unit

Country
ASCO GU
Not Confirmed
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Central Procurement & Supplies Unit

Country
arrow
ASCO GU
Not Confirmed

Goserelin

Brand Name : Zoladex

Dosage Form : Implant

Dosage Strength : 3.6MG

Packaging :

Approval Date : 2020-06-08

Application Number :

Regulatory Info : Invalid

Registration Country : Malta

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17

UAB Boston Biopharma LT

Country
ASCO GU
Not Confirmed
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UAB Boston Biopharma LT

Country
arrow
ASCO GU
Not Confirmed

Goserelin Acetate

Brand Name : Goserelin Uab Boston Biopharma Lt

Dosage Form : Implant

Dosage Strength : 3.6MG

Packaging :

Approval Date : 2019-04-03

Application Number :

Regulatory Info : Withdrawn

Registration Country : Malta

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18

UAB Boston Biopharma LT

Country
ASCO GU
Not Confirmed
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UAB Boston Biopharma LT

Country
arrow
ASCO GU
Not Confirmed

Goserelin Acetate

Brand Name : Goserelin Uab Boston Biopharma Lt

Dosage Form : Implant

Dosage Strength : 10.8MG

Packaging :

Approval Date : 2019-04-03

Application Number :

Regulatory Info : Withdrawn

Registration Country : Malta

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19

Farmagon

Country
ASCO GU
Not Confirmed
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Farmagon

Country
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ASCO GU
Not Confirmed

Goserelin acetate

Brand Name : Zoladex

Dosage Form : Implant

Dosage Strength : 10.8mg

Packaging :

Approval Date :

Application Number :

Regulatory Info : Not Marketed

Registration Country : Norway

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20

Farmagon

Country
ASCO GU
Not Confirmed
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Farmagon

Country
arrow
ASCO GU
Not Confirmed

Goserelin acetate

Brand Name : Zoladex

Dosage Form : Implant

Dosage Strength : 10.8mg

Packaging :

Approval Date :

Application Number :

Regulatory Info : Not Marketed

Registration Country : Norway

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