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    DRL offers a portfolio of products & services, including APIs, CMO services, generics, biosimilars & differentiated formulations.

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    Valsynthese, part of the SSE Group, is a CDMO focused on highly energetic and highly hazardous chemistry.

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    xyz-pharma-m-2024-10-07

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    With Fermion, start the journey of your innovative API.

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    Bloomage is a one-stop source for CEP Sodium Hyaluronate and Hyaluronic Acid// FDA-inspected & GMP-certified.

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    xyz-pharma-m-2024-10-07

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    Butenafine Hydrochloride

    ACTIVE PHARMA INGREDIENTS

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    01 1BAYER HEALTHCARE LLC

    02 1MYLAN BERTEK

    03 2NORVIUM BIOSCIENCE

    04 1TARO

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    01

    BAYER HEALTHCARE LLC

    Germany
    Pharma, Lab & Chemical Expo
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    BAYER HEALTHCARE LLC

    Germany
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    RLD : Yes

    TE Code :

    BUTENAFINE HYDROCHLORIDE

    Brand Name : LOTRIMIN ULTRA

    Dosage Form : CREAM;TOPICAL

    Dosage Strength : 1%

    Approval Date : 2001-12-07

    Application Number : 21307

    RX/OTC/DISCN : OTC

    RLD : Yes

    TE Code :

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    02

    TARO

    U.S.A
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    TARO

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    RLD : No

    TE Code :

    BUTENAFINE HYDROCHLORIDE

    Brand Name : BUTENAFINE HYDROCHLORIDE

    Dosage Form : CREAM;TOPICAL

    Dosage Strength : 1%

    Approval Date : 2017-11-16

    Application Number : 205181

    RX/OTC/DISCN : OTC

    RLD : No

    TE Code :

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    03

    MYLAN BERTEK

    U.S.A
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    MYLAN BERTEK

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    TE Code :

    BUTENAFINE HYDROCHLORIDE

    Brand Name : MENTAX

    Dosage Form : CREAM; TOPICAL

    Dosage Strength : 1%

    Approval Date :

    Application Number : 20663

    RX/OTC/DISCN :

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    TE Code :

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    NORVIUM BIOSCIENCE

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    NORVIUM BIOSCIENCE

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    RLD : Yes

    TE Code :

    BUTENAFINE HYDROCHLORIDE

    Brand Name : MENTAX

    Dosage Form : CREAM;TOPICAL

    Dosage Strength : 1%

    Approval Date : 1996-10-18

    Application Number : 20524

    RX/OTC/DISCN : DISCN

    RLD : Yes

    TE Code :

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    NORVIUM BIOSCIENCE

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    NORVIUM BIOSCIENCE

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    RLD : No

    TE Code :

    BUTENAFINE HYDROCHLORIDE

    Brand Name : MENTAX-TC

    Dosage Form : CREAM;TOPICAL

    Dosage Strength : 1%

    Approval Date : 2002-10-17

    Application Number : 21408

    RX/OTC/DISCN : DISCN

    RLD : No

    TE Code :

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