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    Polpharma is a Polish CDMO of APIs and a significant European API producer, delivering products to companies worldwide.

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    SPI Pharma has been solving formulation challenges using superior functional materials.

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    Granules India Limited has high volume world-class facilities for APIs, PFIs, & FDFs, serving customers in over 80 countries.

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    Erlotinib Hydrochloride

    ACTIVE PHARMA INGREDIENTS

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    01 3Accord healthcare

    02 3Alembic Pharmaceuticals Limited

    03 6Apotex Inc

    04 3Astellas Pharma

    05 3Aurobindo Pharma Limited

    06 2Chartwell Pharmaceuticals llc

    07 3Cipla Medpro South Africa

    08 3Eurolab

    09 6F. Hoffmann-La Roche

    10 2Fujian South Pharmaceutical

    11 5Hetero Drugs

    12 3MSN Laboratories

    13 3Natco Pharma

    14 3Natco Pharma (Canada) Inc

    15 2Nishchay Pharmaceuticals Pvt. Ltd.

    16 2Pharmascience Inc.

    17 3Rising Pharmaceuticals Inc

    18 3Shilpa Medicare

    19 3Sun Pharmaceutical Industries Limited

    20 6Teva Pharmaceutical Industries

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    01

    Accord healthcare

    United Kingdom
    MAGHREB PHARMA
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    ERLOTINIB HYDROCHLORIDE

    Brand Name : ERLOTINIB HYDROCHLORIDE

    Dosage Form : TABLET;ORAL

    Dosage Strength : EQ 25MG BASE

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    Approval Date : 2020-07-02

    Application Number : 211083

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    Accord healthcare

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    Accord healthcare

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    ERLOTINIB HYDROCHLORIDE

    Brand Name : ERLOTINIB HYDROCHLORIDE

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    Apotex Inc

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    ERLOTINIB HYDROCHLORIDE

    Brand Name : ERLOTINIB HYDROCHLORIDE

    Dosage Form : TABLET;ORAL

    Dosage Strength : EQ 25MG BASE

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    Approval Date : 2019-11-05

    Application Number : 208396

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    05

    Apotex Inc

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    ERLOTINIB HYDROCHLORIDE

    Brand Name : ERLOTINIB HYDROCHLORIDE

    Dosage Form : TABLET;ORAL

    Dosage Strength : EQ 100MG BASE

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    Approval Date : 2019-11-05

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    06

    Apotex Inc

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    ERLOTINIB HYDROCHLORIDE

    Brand Name : ERLOTINIB HYDROCHLORIDE

    Dosage Form : TABLET;ORAL

    Dosage Strength : EQ 150MG BASE

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    Approval Date : 2019-11-05

    Application Number : 208396

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    Registration Country : USA

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    07

    Astellas Pharma

    Japan
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    ERLOTINIB HYDROCHLORIDE

    Brand Name : TARCEVA

    Dosage Form : TABLET;ORAL

    Dosage Strength : EQ 25MG BASE **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons**

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    Approval Date : 2004-11-18

    Application Number : 21743

    Regulatory Info : DISCN

    Registration Country : USA

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    08

    Astellas Pharma

    Japan
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    ERLOTINIB HYDROCHLORIDE

    Brand Name : TARCEVA

    Dosage Form : TABLET;ORAL

    Dosage Strength : EQ 100MG BASE **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons**

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    Approval Date : 2004-11-18

    Application Number : 21743

    Regulatory Info : DISCN

    Registration Country : USA

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    09

    Astellas Pharma

    Japan
    MAGHREB PHARMA
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    Astellas Pharma

    Japan
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    MAGHREB PHARMA
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    ERLOTINIB HYDROCHLORIDE

    Brand Name : TARCEVA

    Dosage Form : TABLET;ORAL

    Dosage Strength : EQ 150MG BASE **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons**

    Packaging :

    Approval Date : 2004-11-18

    Application Number : 21743

    Regulatory Info : DISCN

    Registration Country : USA

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    10

    Chartwell Pharmaceuticals llc

    U.S.A
    MAGHREB PHARMA
    Not Confirmed
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    Chartwell Pharmaceuticals llc

    U.S.A
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    MAGHREB PHARMA
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    ERLOTINIB HYDROCHLORIDE

    Brand Name : ERLOTINIB HYDROCHLORIDE

    Dosage Form : TABLET;ORAL

    Dosage Strength : EQ 25MG BASE

    Packaging :

    Approval Date : 2024-09-13

    Application Number : 203843

    Regulatory Info : RX

    Registration Country : USA

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    11

    Chartwell Pharmaceuticals llc

    U.S.A
    MAGHREB PHARMA
    Not Confirmed
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    Chartwell Pharmaceuticals llc

    U.S.A
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    MAGHREB PHARMA
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    ERLOTINIB HYDROCHLORIDE

    Brand Name : ERLOTINIB HYDROCHLORIDE

    Dosage Form : TABLET;ORAL

    Dosage Strength : EQ 150MG BASE

    Packaging :

    Approval Date : 2024-09-13

    Application Number : 203843

    Regulatory Info : RX

    Registration Country : USA

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    12

    Hetero Drugs

    India
    MAGHREB PHARMA
    Not Confirmed
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    Hetero Drugs

    India
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    MAGHREB PHARMA
    Not Confirmed
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    Brand Name : ERLOTINIB HYDROCHLORIDE

    Dosage Form : TABLET;ORAL

    Dosage Strength : EQ 25MG BASE

    Packaging :

    Approval Date : 2024-05-24

    Application Number : 209267

    Regulatory Info : RX

    Registration Country : USA

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    13

    Hetero Drugs

    India
    MAGHREB PHARMA
    Not Confirmed
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    Hetero Drugs

    India
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    MAGHREB PHARMA
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    ERLOTINIB HYDROCHLORIDE

    Brand Name : ERLOTINIB HYDROCHLORIDE

    Dosage Form : TABLET;ORAL

    Dosage Strength : EQ 100MG BASE

    Packaging :

    Approval Date : 2024-05-24

    Application Number : 209267

    Regulatory Info : RX

    Registration Country : USA

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    14

    Hetero Drugs

    India
    MAGHREB PHARMA
    Not Confirmed
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    India
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    MAGHREB PHARMA
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    Brand Name : ERLOTINIB HYDROCHLORIDE

    Dosage Form : TABLET;ORAL

    Dosage Strength : EQ 150MG BASE

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    Approval Date : 2024-05-24

    Application Number : 209267

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    Registration Country : USA

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    15

    Natco Pharma

    India
    MAGHREB PHARMA
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    Natco Pharma

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    Brand Name : ERLOTINIB HYDROCHLORIDE

    Dosage Form : TABLET;ORAL

    Dosage Strength : EQ 25MG BASE

    Packaging :

    Approval Date : 2019-11-05

    Application Number : 208488

    Regulatory Info : DISCN

    Registration Country : USA

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    Natco Pharma

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    Natco Pharma

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    Brand Name : ERLOTINIB HYDROCHLORIDE

    Dosage Form : TABLET;ORAL

    Dosage Strength : EQ 100MG BASE

    Packaging :

    Approval Date : 2019-11-05

    Application Number : 208488

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    Registration Country : USA

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    Natco Pharma

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    Brand Name : ERLOTINIB HYDROCHLORIDE

    Dosage Form : TABLET;ORAL

    Dosage Strength : EQ 150MG BASE

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    Approval Date : 2019-11-05

    Application Number : 208488

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    Registration Country : USA

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    18

    Rising Pharmaceuticals Inc

    U.S.A
    MAGHREB PHARMA
    Not Confirmed
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    Rising Pharmaceuticals Inc

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    Brand Name : ERLOTINIB HYDROCHLORIDE

    Dosage Form : TABLET;ORAL

    Dosage Strength : EQ 25MG BASE

    Packaging :

    Approval Date : 2014-06-11

    Application Number : 91002

    Regulatory Info : RX

    Registration Country : USA

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    19

    Rising Pharmaceuticals Inc

    U.S.A
    MAGHREB PHARMA
    Not Confirmed
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    Rising Pharmaceuticals Inc

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    MAGHREB PHARMA
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    Brand Name : ERLOTINIB HYDROCHLORIDE

    Dosage Form : TABLET;ORAL

    Dosage Strength : EQ 100MG BASE

    Packaging :

    Approval Date : 2014-06-11

    Application Number : 91002

    Regulatory Info : RX

    Registration Country : USA

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    Rising Pharmaceuticals Inc

    U.S.A
    MAGHREB PHARMA
    Not Confirmed
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    Rising Pharmaceuticals Inc

    U.S.A
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    Brand Name : ERLOTINIB HYDROCHLORIDE

    Dosage Form : TABLET;ORAL

    Dosage Strength : EQ 150MG BASE

    Packaging :

    Approval Date : 2014-06-11

    Application Number : 91002

    Regulatory Info : RX

    Registration Country : USA

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    21

    Shilpa Medicare

    India
    MAGHREB PHARMA
    Not Confirmed
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    Shilpa Medicare

    India
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    MAGHREB PHARMA
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    Brand Name : ERLOTINIB HYDROCHLORIDE

    Dosage Form : TABLET;ORAL

    Dosage Strength : EQ 25MG BASE

    Packaging :

    Approval Date : 2019-11-05

    Application Number : 211960

    Regulatory Info : RX

    Registration Country : USA

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    Shilpa Medicare

    India
    MAGHREB PHARMA
    Not Confirmed
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    Shilpa Medicare

    India
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    MAGHREB PHARMA
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    Brand Name : ERLOTINIB HYDROCHLORIDE

    Dosage Form : TABLET;ORAL

    Dosage Strength : EQ 100MG BASE

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    Approval Date : 2019-11-05

    Application Number : 211960

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    Shilpa Medicare

    India
    MAGHREB PHARMA
    Not Confirmed
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    Shilpa Medicare

    India
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    MAGHREB PHARMA
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    Brand Name : ERLOTINIB HYDROCHLORIDE

    Dosage Form : TABLET;ORAL

    Dosage Strength : EQ 150MG BASE

    Packaging :

    Approval Date : 2019-11-05

    Application Number : 211960

    Regulatory Info : RX

    Registration Country : USA

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    Sun Pharmaceutical Industries Limit...

    India
    MAGHREB PHARMA
    Not Confirmed
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    Sun Pharmaceutical Industries Limit...

    India
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    MAGHREB PHARMA
    Not Confirmed
    • fda
    • EDQM
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    Regulatory Info : DISCN

    Registration Country : USA

    ERLOTINIB HYDROCHLORIDE

    Brand Name : ERLOTINIB HYDROCHLORIDE

    Dosage Form : TABLET;ORAL

    Dosage Strength : EQ 25MG BASE

    Packaging :

    Approval Date : 2019-11-05

    Application Number : 210300

    Regulatory Info : DISCN

    Registration Country : USA

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    25

    Sun Pharmaceutical Industries Limit...

    India
    MAGHREB PHARMA
    Not Confirmed
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    Sun Pharmaceutical Industries Limit...

    India
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    MAGHREB PHARMA
    Not Confirmed
    • fda
    • EDQM
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    Regulatory Info : DISCN

    Registration Country : USA

    ERLOTINIB HYDROCHLORIDE

    Brand Name : ERLOTINIB HYDROCHLORIDE

    Dosage Form : TABLET;ORAL

    Dosage Strength : EQ 100MG BASE

    Packaging :

    Approval Date : 2019-11-05

    Application Number : 210300

    Regulatory Info : DISCN

    Registration Country : USA

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    26

    Sun Pharmaceutical Industries Limit...

    India
    MAGHREB PHARMA
    Not Confirmed
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    Sun Pharmaceutical Industries Limit...

    India
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    MAGHREB PHARMA
    Not Confirmed
    • fda
    • EDQM
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    Regulatory Info : DISCN

    Registration Country : USA

    ERLOTINIB HYDROCHLORIDE

    Brand Name : ERLOTINIB HYDROCHLORIDE

    Dosage Form : TABLET;ORAL

    Dosage Strength : EQ 150MG BASE

    Packaging :

    Approval Date : 2019-11-05

    Application Number : 210300

    Regulatory Info : DISCN

    Registration Country : USA

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    27

    Teva Pharmaceutical Industries

    Israel
    MAGHREB PHARMA
    Not Confirmed
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    Teva Pharmaceutical Industries

    Israel
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    MAGHREB PHARMA
    Not Confirmed
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    Regulatory Info : RX

    Registration Country : USA

    ERLOTINIB HYDROCHLORIDE

    Brand Name : ERLOTINIB HYDROCHLORIDE

    Dosage Form : TABLET;ORAL

    Dosage Strength : EQ 25MG BASE

    Packaging :

    Approval Date : 2020-11-09

    Application Number : 91059

    Regulatory Info : RX

    Registration Country : USA

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    28

    Teva Pharmaceutical Industries

    Israel
    MAGHREB PHARMA
    Not Confirmed
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    Teva Pharmaceutical Industries

    Israel
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    MAGHREB PHARMA
    Not Confirmed
    • fda
    • EDQM
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    Regulatory Info : RX

    Registration Country : USA

    ERLOTINIB HYDROCHLORIDE

    Brand Name : ERLOTINIB HYDROCHLORIDE

    Dosage Form : TABLET;ORAL

    Dosage Strength : EQ 100MG BASE

    Packaging :

    Approval Date : 2015-08-28

    Application Number : 91059

    Regulatory Info : RX

    Registration Country : USA

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    29

    Teva Pharmaceutical Industries

    Israel
    MAGHREB PHARMA
    Not Confirmed
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    Teva Pharmaceutical Industries

    Israel
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    MAGHREB PHARMA
    Not Confirmed
    • fda
    • EDQM
    • WHO-GMP
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    Regulatory Info : RX

    Registration Country : USA

    ERLOTINIB HYDROCHLORIDE

    Brand Name : ERLOTINIB HYDROCHLORIDE

    Dosage Form : TABLET;ORAL

    Dosage Strength : EQ 150MG BASE

    Packaging :

    Approval Date : 2015-08-28

    Application Number : 91059

    Regulatory Info : RX

    Registration Country : USA

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    30

    Zydus Pharmaceuticals

    U.S.A
    MAGHREB PHARMA
    Not Confirmed
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    Zydus Pharmaceuticals

    U.S.A
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    MAGHREB PHARMA
    Not Confirmed
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    • EDQM
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    Regulatory Info : RX

    Registration Country : USA

    ERLOTINIB HYDROCHLORIDE

    Brand Name : ERLOTINIB HYDROCHLORIDE

    Dosage Form : TABLET;ORAL

    Dosage Strength : EQ 25MG BASE

    Packaging :

    Approval Date : 2020-04-16

    Application Number : 213065

    Regulatory Info : RX

    Registration Country : USA

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