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    ChemWerth works in generic API development & supply, non-infringement patent strategy development and regulatory support.

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    Centrient is a leading manufacturer of Beta-Lactam Antibiotics and a provider of next-generation Statins and Antifungals.

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    Bachem Group is a public, innovation-driven company specializing in the development and manufacturing of peptides and oligonucleotides.

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    Eletriptan Hydrobromide

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    01 2Orion Corporation

    02 32care4

    03 3Alter Nova

    04 2Annora Pharma

    05 4Apotex Inc

    06 2Auro Pharma Inc

    07 7Aurobindo Pharma Limited

    08 2Aurovitas Spain, Sau

    09 2Axapharm

    10 2BGP PHARMA ULC

    11 2Beximco Pharmaceuticals

    12 2Bluefish Pharmaceuticals AB

    13 2Chartwell Pharmaceuticals llc

    14 1DIFARMED S.L.

    15 2DOC Generici

    16 1EG Spa

    17 2EQL Pharma

    18 2Ebb Medical

    19 3Farm Agon

    20 2Jerome Stevens Pharmaceuticals

    21 2Mepha Pharma

    22 6ORIFARM GROUP AS

    23 2PRO DOC LIMITEE

    24 2Paranova Pharmaceuticals Ab

    25 2Pensa Pharma

    26 15Pfizer Inc

    27 2Pharmascience Inc.

    28 2SANIS HEALTH INC

    29 2Spirig Healthcare

    30 6Teva Pharmaceutical Industries

    31 20Viatris

    32 3Viatris Healthcare (Pty) Ltd

    33 2Yung Shin Pharm Industrial

    34 2Zydus Pharmaceuticals

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    01

    Orion Corporation

    Finland
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    Regulatory Info : Approved

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    Eletriptanhydrobromid

    Brand Name : Eletriptan Orion

    Dosage Form : Film Coated Tablet

    Dosage Strength : 20mg

    Packaging :

    Approval Date : 02/10/2018

    Application Number : 20171006000043

    Regulatory Info : Approved

    Registration Country : Sweden

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    02

    Orion Corporation

    Finland
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    Regulatory Info : Approved

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    Eletriptanhydrobromid

    Brand Name : Eletriptan Orion

    Dosage Form : Film Coated Tablet

    Dosage Strength : 40mg

    Packaging :

    Approval Date : 02/10/2018

    Application Number : 20171006000050

    Regulatory Info : Approved

    Registration Country : Sweden

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    03

    Apotex Inc

    Canada
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    ELETRIPTAN HYDROBROMIDE

    Brand Name : ELETRIPTAN HYDROBROMIDE

    Dosage Form : TABLET; ORAL

    Dosage Strength : 20MG

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    Approval Date :

    Application Number : 201536

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    Registration Country : USA

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    04

    Apotex Inc

    Canada
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    Registration Country : USA

    ELETRIPTAN HYDROBROMIDE

    Brand Name : ELETRIPTAN HYDROBROMIDE

    Dosage Form : TABLET; ORAL

    Dosage Strength : 40MG

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    Application Number : 201536

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    Registration Country : USA

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    05

    Aurobindo Pharma Limited

    India
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    India
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    Regulatory Info : RX

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    ELETRIPTAN HYDROBROMIDE

    Brand Name : ELETRIPTAN HYDROBROMIDE

    Dosage Form : TABLET;ORAL

    Dosage Strength : EQ 20MG BASE

    Packaging :

    Approval Date : 2019-01-15

    Application Number : 210708

    Regulatory Info : RX

    Registration Country : USA

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    06

    Aurobindo Pharma Limited

    India
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    ELETRIPTAN HYDROBROMIDE

    Brand Name : ELETRIPTAN HYDROBROMIDE

    Dosage Form : TABLET;ORAL

    Dosage Strength : EQ 40MG BASE

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    Approval Date : 2019-01-15

    Application Number : 210708

    Regulatory Info : RX

    Registration Country : USA

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    07

    Chartwell Pharmaceuticals llc

    U.S.A
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    Chartwell Pharmaceuticals llc

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    ELETRIPTAN HYDROBROMIDE

    Brand Name : ELETRIPTAN HYDROBROMIDE

    Dosage Form : TABLET;ORAL

    Dosage Strength : EQ 20MG BASE

    Packaging :

    Approval Date : 2017-08-29

    Application Number : 205186

    Regulatory Info : RX

    Registration Country : USA

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    08

    Chartwell Pharmaceuticals llc

    U.S.A
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    ELETRIPTAN HYDROBROMIDE

    Brand Name : ELETRIPTAN HYDROBROMIDE

    Dosage Form : TABLET;ORAL

    Dosage Strength : EQ 40MG BASE

    Packaging :

    Approval Date : 2017-08-29

    Application Number : 205186

    Regulatory Info : RX

    Registration Country : USA

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    09

    Jerome Stevens Pharmaceuticals

    U.S.A
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    Jerome Stevens Pharmaceuticals

    U.S.A
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    Regulatory Info : DISCN

    Registration Country : USA

    ELETRIPTAN HYDROBROMIDE

    Brand Name : ELETRIPTAN HYDROBROMIDE

    Dosage Form : TABLET;ORAL

    Dosage Strength : EQ 20MG BASE

    Packaging :

    Approval Date : 2018-05-25

    Application Number : 206787

    Regulatory Info : DISCN

    Registration Country : USA

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    10

    Jerome Stevens Pharmaceuticals

    U.S.A
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    Jerome Stevens Pharmaceuticals

    U.S.A
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    Regulatory Info : DISCN

    Registration Country : USA

    ELETRIPTAN HYDROBROMIDE

    Brand Name : ELETRIPTAN HYDROBROMIDE

    Dosage Form : TABLET;ORAL

    Dosage Strength : EQ 40MG BASE

    Packaging :

    Approval Date : 2018-05-25

    Application Number : 206787

    Regulatory Info : DISCN

    Registration Country : USA

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    11

    Pfizer Inc

    U.S.A
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    Pfizer Inc

    U.S.A
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    Regulatory Info : RX

    Registration Country : USA

    ELETRIPTAN HYDROBROMIDE

    Brand Name : RELPAX

    Dosage Form : TABLET;ORAL

    Dosage Strength : EQ 20MG BASE

    Packaging :

    Approval Date : 2002-12-26

    Application Number : 21016

    Regulatory Info : RX

    Registration Country : USA

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    12

    Pfizer Inc

    U.S.A
    The MedTech Conference
    Not Confirmed
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    Pfizer Inc

    U.S.A
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    Regulatory Info : RX

    Registration Country : USA

    ELETRIPTAN HYDROBROMIDE

    Brand Name : RELPAX

    Dosage Form : TABLET;ORAL

    Dosage Strength : EQ 40MG BASE

    Packaging :

    Approval Date : 2002-12-26

    Application Number : 21016

    Regulatory Info : RX

    Registration Country : USA

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    13

    Teva Pharmaceutical Industries

    Israel
    The MedTech Conference
    Not Confirmed
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    Teva Pharmaceutical Industries

    Israel
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    Regulatory Info : RX

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    ELETRIPTAN HYDROBROMIDE

    Brand Name : ELETRIPTAN HYDROBROMIDE

    Dosage Form : TABLET;ORAL

    Dosage Strength : EQ 20MG BASE

    Packaging :

    Approval Date : 2017-06-27

    Application Number : 202040

    Regulatory Info : RX

    Registration Country : USA

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    14

    Teva Pharmaceutical Industries

    Israel
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    Israel
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    Regulatory Info : RX

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    ELETRIPTAN HYDROBROMIDE

    Brand Name : ELETRIPTAN HYDROBROMIDE

    Dosage Form : TABLET;ORAL

    Dosage Strength : EQ 40MG BASE

    Packaging :

    Approval Date : 2017-06-27

    Application Number : 202040

    Regulatory Info : RX

    Registration Country : USA

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    15

    Viatris

    U.S.A
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    Viatris

    U.S.A
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    Regulatory Info : RX

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    ELETRIPTAN HYDROBROMIDE

    Brand Name : ELETRIPTAN HYDROBROMIDE

    Dosage Form : TABLET;ORAL

    Dosage Strength : EQ 20MG BASE

    Packaging :

    Approval Date : 2017-08-11

    Application Number : 205152

    Regulatory Info : RX

    Registration Country : USA

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    16

    Viatris

    U.S.A
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    Viatris

    U.S.A
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    Brand Name : ELETRIPTAN HYDROBROMIDE

    Dosage Form : TABLET;ORAL

    Dosage Strength : EQ 40MG BASE

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    Approval Date : 2017-08-11

    Application Number : 205152

    Regulatory Info : RX

    Registration Country : USA

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    17

    Yung Shin Pharm Industrial

    Taiwan
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    Taiwan
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    Brand Name : ELETRIPTAN HYDROBROMIDE

    Dosage Form : TABLET;ORAL

    Dosage Strength : EQ 20MG BASE

    Packaging :

    Approval Date : 2020-07-13

    Application Number : 209680

    Regulatory Info : DISCN

    Registration Country : USA

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    18

    Yung Shin Pharm Industrial

    Taiwan
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    Brand Name : ELETRIPTAN HYDROBROMIDE

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    Dosage Strength : EQ 40MG BASE

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    Approval Date : 2020-07-13

    Application Number : 209680

    Regulatory Info : DISCN

    Registration Country : USA

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    19

    Zydus Pharmaceuticals

    U.S.A
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    Zydus Pharmaceuticals

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    ELETRIPTAN HYDROBROMIDE

    Brand Name : ELETRIPTAN HYDROBROMIDE

    Dosage Form : TABLET;ORAL

    Dosage Strength : EQ 20MG BASE

    Packaging :

    Approval Date : 2017-06-16

    Application Number : 206409

    Regulatory Info : RX

    Registration Country : USA

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    20

    Zydus Pharmaceuticals

    U.S.A
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    ELETRIPTAN HYDROBROMIDE

    Brand Name : ELETRIPTAN HYDROBROMIDE

    Dosage Form : TABLET;ORAL

    Dosage Strength : EQ 40MG BASE

    Packaging :

    Approval Date : 2017-06-16

    Application Number : 206409

    Regulatory Info : RX

    Registration Country : USA

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