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    Biophore is a research-driven global pharmaceutical company focused on niche APIs for the generic industry.

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    TransoPharm USA works in the Sourcing and Management of Active Pharmaceutical Ingredients.

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    xyz-pharma-m-2025-01-06

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    LEBSA- Your strategic API source for niche molecules.

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    Nuray is an expert in the synthesis of Niche novel APIs, the first to launch Generics, NCEs, Advanced Intermediates // USFDA certified.

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    NAFTIFINE HCL

    ACTIVE PHARMA INGREDIENTS

    INTERMEDIATES

    FINISHED DOSAGE FORMULATIONS

    DRUG PRODUCT COMPOSITIONS

    RELATED EXCIPIENT COMPANIES

    EXCIPIENTS BY APPLICATIONS

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    01 2AMNEAL

    02 4LEGACY PHARMA

    03 3TARO

    04 1XIROMED

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    01

    AMNEAL

    U.S.A
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    AMNEAL

    U.S.A
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    RLD : No

    TE Code : AB

    NAFTIFINE HYDROCHLORIDE

    Brand Name : NAFTIFINE HYDROCHLORIDE

    Dosage Form : GEL;TOPICAL

    Dosage Strength : 1%

    Approval Date : 2019-03-20

    Application Number : 206165

    RX/OTC/DISCN : RX

    RLD : No

    TE Code : AB

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    02

    AMNEAL

    U.S.A
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    AMNEAL

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    RLD : No

    TE Code : AB

    NAFTIFINE HYDROCHLORIDE

    Brand Name : NAFTIFINE HYDROCHLORIDE

    Dosage Form : CREAM;TOPICAL

    Dosage Strength : 2%

    Approval Date : 2017-04-10

    Application Number : 206960

    RX/OTC/DISCN : RX

    RLD : No

    TE Code : AB

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    03

    LEGACY PHARMA

    Barbados
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    LEGACY PHARMA

    Barbados
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    Duphat
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    RLD : Yes

    TE Code : AB

    NAFTIFINE HYDROCHLORIDE

    Brand Name : NAFTIN

    Dosage Form : GEL;TOPICAL

    Dosage Strength : 1%

    Approval Date : 1990-06-18

    Application Number : 19356

    RX/OTC/DISCN : RX

    RLD : Yes

    TE Code : AB

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    04

    LEGACY PHARMA

    Barbados
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    LEGACY PHARMA

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    RLD : Yes

    TE Code :

    NAFTIFINE HYDROCHLORIDE

    Brand Name : NAFTIN

    Dosage Form : CREAM;TOPICAL

    Dosage Strength : 1% **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons**

    Approval Date : 1988-02-29

    Application Number : 19599

    RX/OTC/DISCN : DISCN

    RLD : Yes

    TE Code :

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    05

    LEGACY PHARMA

    Barbados
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    LEGACY PHARMA

    Barbados
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    Duphat
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    RLD : Yes

    TE Code : AB

    NAFTIFINE HYDROCHLORIDE

    Brand Name : NAFTIN

    Dosage Form : CREAM;TOPICAL

    Dosage Strength : 2%

    Approval Date : 2012-01-13

    Application Number : 19599

    RX/OTC/DISCN : RX

    RLD : Yes

    TE Code : AB

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    06

    LEGACY PHARMA

    Barbados
    Duphat
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    LEGACY PHARMA

    Barbados
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    Duphat
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    RLD : Yes

    TE Code : AB

    NAFTIFINE HYDROCHLORIDE

    Brand Name : NAFTIN

    Dosage Form : GEL;TOPICAL

    Dosage Strength : 2%

    Approval Date : 2013-06-27

    Application Number : 204286

    RX/OTC/DISCN : RX

    RLD : Yes

    TE Code : AB

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    07

    TARO

    U.S.A
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    TARO

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    RLD : No

    TE Code :

    NAFTIFINE HYDROCHLORIDE

    Brand Name : NAFTIFINE HYDROCHLORIDE

    Dosage Form : CREAM;TOPICAL

    Dosage Strength : 1%

    Approval Date : 2016-09-08

    Application Number : 205975

    RX/OTC/DISCN : RX

    RLD : No

    TE Code :

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    08

    TARO

    U.S.A
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    TARO

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    RLD : No

    TE Code : AB

    NAFTIFINE HYDROCHLORIDE

    Brand Name : NAFTIFINE HYDROCHLORIDE

    Dosage Form : CREAM;TOPICAL

    Dosage Strength : 2%

    Approval Date : 2016-01-06

    Application Number : 206901

    RX/OTC/DISCN : RX

    RLD : No

    TE Code : AB

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    09

    TARO

    U.S.A
    Duphat
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    TARO

    U.S.A
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    Duphat
    Not Confirmed
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    RLD : No

    TE Code : AB

    NAFTIFINE HYDROCHLORIDE

    Brand Name : NAFTIFINE HYDROCHLORIDE

    Dosage Form : GEL;TOPICAL

    Dosage Strength : 2%

    Approval Date : 2019-04-10

    Application Number : 208201

    RX/OTC/DISCN : RX

    RLD : No

    TE Code : AB

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    10

    XIROMED

    U.S.A
    Duphat
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    XIROMED

    U.S.A
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    Duphat
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    RLD : No

    TE Code : AB

    NAFTIFINE HYDROCHLORIDE

    Brand Name : NAFTIFINE HYDROCHLORIDE

    Dosage Form : CREAM;TOPICAL

    Dosage Strength : 2%

    Approval Date : 2020-09-22

    Application Number : 210038

    RX/OTC/DISCN : RX

    RLD : No

    TE Code : AB

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