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    AbbVie CDMO has been working with global companies to develop, manufacture & scale biopharmaceutical products.

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    End-to-end drug development, specializing in high-potency softgels and liquids, providing global partners with a competitive advantage.

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    Kewpie is your partner for Sodium Hyaluronate & Hyaluronic Acid// CEP, USDMF, KDMF & JDMF registered.

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    Erlotinib Hydrochloride

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    06 2Chartwell Pharmaceuticals llc

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    01

    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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    ERLOTINIB HYDROCHLORIDE

    Brand Name : ERLOTINIB HYDROCHLORIDE

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    ERLOTINIB HYDROCHLORIDE

    Brand Name : ERLOTINIB HYDROCHLORIDE

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    Dosage Strength : EQ 25MG BASE **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons**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

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    Dosage Strength : EQ 100MG BASE **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons**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

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    Astellas Pharma

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    ERLOTINIB HYDROCHLORIDE

    Brand Name : TARCEVA

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    Dosage Strength : EQ 150MG BASE **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons**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

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    Chartwell Pharmaceuticals llc

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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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    Registration Country : USA

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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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    09

    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

    Regulatory Info : RX

    Registration Country : USA

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    10

    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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    Registration Country : USA

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    11

    Hetero Drugs

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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

    Regulatory Info : RX

    Registration Country : USA

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    12

    Natco 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 : 2019-11-05

    Application Number : 208488

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    Registration Country : USA

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    Natco Pharma

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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

    Application Number : 208488

    Regulatory Info : DISCN

    Registration Country : USA

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    14

    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

    Regulatory Info : DISCN

    Registration Country : USA

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    15

    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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    Rising Pharmaceuticals Inc

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    Brand Name : ERLOTINIB HYDROCHLORIDE

    Dosage Form : TABLET;ORAL

    Dosage Strength : EQ 100MG BASE

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    Approval Date : 2014-06-11

    Application Number : 91002

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    Registration Country : USA

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    17

    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

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    Registration Country : USA

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    18

    Teva Pharmaceutical Industries

    Israel
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    Brand Name : ERLOTINIB HYDROCHLORIDE

    Dosage Form : TABLET;ORAL

    Dosage Strength : EQ 25MG BASE

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    Approval Date : 2020-11-09

    Application Number : 91059

    Regulatory Info : RX

    Registration Country : USA

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    Teva Pharmaceutical Industries

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    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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    Teva Pharmaceutical Industries

    Israel
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    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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