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    Erlotinib Hydrochloride

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    Accord healthcare

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    ERLOTINIB HYDROCHLORIDE

    Brand Name : ERLOTINIB HYDROCHLORIDE

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    Brand Name : ERLOTINIB HYDROCHLORIDE

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    Approval Date : 2019-11-05

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    Apotex Inc

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    Apotex Inc

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    ERLOTINIB HYDROCHLORIDE

    Brand Name : TARCEVA

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    Dosage Strength : EQ 25MG BASE **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons**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

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    Brand Name : TARCEVA

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    Dosage Strength : EQ 100MG BASE **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons**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

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    09

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    Dosage Strength : EQ 150MG BASE **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons**

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    Approval Date : 2004-11-18

    Application Number : 21743

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    10

    Chartwell Pharmaceuticals llc

    U.S.A
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    Brand Name : ERLOTINIB HYDROCHLORIDE

    Dosage Form : TABLET;ORAL

    Dosage Strength : EQ 25MG BASE

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    Approval Date : 2024-09-13

    Application Number : 203843

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    Chartwell Pharmaceuticals llc

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    Brand Name : ERLOTINIB HYDROCHLORIDE

    Dosage Form : TABLET;ORAL

    Dosage Strength : EQ 150MG BASE

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    Approval Date : 2024-09-13

    Application Number : 203843

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    12

    Hetero Drugs

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    Brand Name : ERLOTINIB HYDROCHLORIDE

    Dosage Form : TABLET;ORAL

    Dosage Strength : EQ 25MG BASE

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    Approval Date : 2024-05-24

    Application Number : 209267

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    Registration Country : USA

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    13

    Hetero Drugs

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    Brand Name : ERLOTINIB HYDROCHLORIDE

    Dosage Form : TABLET;ORAL

    Dosage Strength : EQ 100MG BASE

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    Approval Date : 2024-05-24

    Application Number : 209267

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    14

    Hetero Drugs

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    Natco Pharma

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    Brand Name : ERLOTINIB HYDROCHLORIDE

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    Approval Date : 2019-11-05

    Application Number : 208488

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    Approval Date : 2019-11-05

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    Approval Date : 2019-11-05

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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

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    Brand Name : ERLOTINIB HYDROCHLORIDE

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    Dosage Strength : EQ 100MG BASE

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    Approval Date : 2014-06-11

    Application Number : 91002

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    Rising Pharmaceuticals Inc

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    Brand Name : ERLOTINIB HYDROCHLORIDE

    Dosage Form : TABLET;ORAL

    Dosage Strength : EQ 150MG BASE

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    Approval Date : 2014-06-11

    Application Number : 91002

    Regulatory Info : RX

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    Shilpa Medicare

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    Brand Name : ERLOTINIB HYDROCHLORIDE

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    Dosage Strength : EQ 25MG BASE

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    Approval Date : 2019-11-05

    Application Number : 211960

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    Shilpa Medicare

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    Approval Date : 2019-11-05

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    Shilpa Medicare

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    Approval Date : 2019-11-05

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    24

    Sun Pharmaceutical Industries Limit...

    India
    Medlab Asia & Asia Health
    Not Confirmed
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    Sun Pharmaceutical Industries Limit...

    India
    arrow
    Medlab Asia & Asia Health
    Not Confirmed
    • fda
    • EDQM
    • WHO-GMP
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    Flag India
    Virtual Booth Virtual Booth
    Digital Content Digital Content

    Regulatory Info : RX

    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 : RX

    Registration Country : USA

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    25

    Sun Pharmaceutical Industries Limit...

    India
    Medlab Asia & Asia Health
    Not Confirmed
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    Sun Pharmaceutical Industries Limit...

    India
    arrow
    Medlab Asia & Asia Health
    Not Confirmed
    • fda
    • EDQM
    • WHO-GMP
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    Virtual Booth Virtual Booth
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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 : 2019-11-05

    Application Number : 210300

    Regulatory Info : RX

    Registration Country : USA

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    26

    Sun Pharmaceutical Industries Limit...

    India
    Medlab Asia & Asia Health
    Not Confirmed
    arrow

    Sun Pharmaceutical Industries Limit...

    India
    arrow
    Medlab Asia & Asia Health
    Not Confirmed
    • fda
    • EDQM
    • WHO-GMP
    Virtual Booth Boost your online visibility by uploading your products, APIs, FDFs, intermediates, excipients, and services for free on PharmaCompass. Rank higher among suppliers and expand your reach across the internet efficiently and cost-effectively.
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    Flag India
    Virtual Booth Virtual Booth
    Digital Content Digital Content

    Regulatory Info : RX

    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 : RX

    Registration Country : USA

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    27

    Teva Pharmaceutical Industries

    Israel
    Medlab Asia & Asia Health
    Not Confirmed
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    Teva Pharmaceutical Industries

    Israel
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    Medlab Asia & Asia Health
    Not Confirmed
    • fda
    • EDQM
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    Virtual Booth Virtual Booth
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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
    Medlab Asia & Asia Health
    Not Confirmed
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    Teva Pharmaceutical Industries

    Israel
    arrow
    Medlab Asia & Asia Health
    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 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
    Medlab Asia & Asia Health
    Not Confirmed
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    Teva Pharmaceutical Industries

    Israel
    arrow
    Medlab Asia & Asia Health
    Not Confirmed
    • fda
    • EDQM
    • WHO-GMP
    Virtual Booth Boost your online visibility by uploading your products, APIs, FDFs, intermediates, excipients, and services for free on PharmaCompass. Rank higher among suppliers and expand your reach across the internet efficiently and cost-effectively.
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    Flag Israel
    Virtual Booth Virtual Booth
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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
    Medlab Asia & Asia Health
    Not Confirmed
    arrow

    Zydus Pharmaceuticals

    U.S.A
    arrow
    Medlab Asia & Asia Health
    Not Confirmed
    • fda
    • EDQM
    • WHO-GMP
    Virtual Booth Boost your online visibility by uploading your products, APIs, FDFs, intermediates, excipients, and services for free on PharmaCompass. Rank higher among suppliers and expand your reach across the internet efficiently and cost-effectively.
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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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