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    EUROAPI, the leading small molecules API player, provides both API sales & CDMO services.

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

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    Interquim comes from an international group of 50 companies active in the pharma, hospital, diagnostics, fine chemicals & feed sectors.

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    Cohance Lifesciences, offers full range of CDMO services for small molecule APIs, intermediates, ADCs, Pellets and Formulations.

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    FAMAR CDMO- From early development to commercial manufacturing.

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    Polfa Tarchomin is a leading Polish pharmaceutical company with 200 year tradition in manufacture and sale of pharmaceutical products.

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    Phenytoin

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    01 1ACTAVIS MID ATLANTIC

    02 1EPIC PHARMA LLC

    03 1PAI HOLDINGS PHARM

    04 1PHARMACIA

    05 1RISING

    06 2TARO

    07 2VIATRIS

    08 2VISTAPHARM LLC

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    01

    ACTAVIS MID ATLANTIC

    Ireland
    BioAsia
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    ACTAVIS MID ATLANTIC

    Ireland
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    RLD : No

    TE Code :

    PHENYTOIN

    Brand Name : PHENYTOIN

    Dosage Form : SUSPENSION;ORAL

    Dosage Strength : 125MG/5ML

    Approval Date : 1992-09-25

    Application Number : 89892

    RX/OTC/DISCN : DISCN

    RLD : No

    TE Code :

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    02

    EPIC PHARMA LLC

    U.S.A
    BioAsia
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    EPIC PHARMA LLC

    U.S.A
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    RLD : No

    TE Code : AB

    PHENYTOIN

    Brand Name : PHENYTOIN

    Dosage Form : TABLET, CHEWABLE;ORAL

    Dosage Strength : 50MG

    Approval Date : 2014-11-28

    Application Number : 40884

    RX/OTC/DISCN : RX

    RLD : No

    TE Code : AB

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    03

    PAI HOLDINGS PHARM

    U.S.A
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    PAI HOLDINGS PHARM

    U.S.A
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    RLD : No

    TE Code :

    PHENYTOIN

    Brand Name : PHENYTOIN

    Dosage Form : SUSPENSION;ORAL

    Dosage Strength : 125MG/5ML

    Approval Date : 2002-04-19

    Application Number : 40420

    RX/OTC/DISCN : DISCN

    RLD : No

    TE Code :

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    04

    PHARMACIA

    U.S.A
    BioAsia
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    PHARMACIA

    U.S.A
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    RLD : Yes

    TE Code : AB

    PHENYTOIN

    Brand Name : DILANTIN

    Dosage Form : TABLET, CHEWABLE;ORAL

    Dosage Strength : 50MG

    Approval Date : 1982-01-01

    Application Number : 84427

    RX/OTC/DISCN : RX

    RLD : Yes

    TE Code : AB

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    05

    TARO

    U.S.A
    BioAsia
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    TARO

    U.S.A
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    RLD : No

    TE Code : AB

    PHENYTOIN

    Brand Name : PHENYTOIN

    Dosage Form : SUSPENSION;ORAL

    Dosage Strength : 125MG/5ML

    Approval Date : 2004-03-08

    Application Number : 40521

    RX/OTC/DISCN : RX

    RLD : No

    TE Code : AB

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    06

    TARO

    U.S.A
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    TARO

    U.S.A
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    RLD : No

    TE Code : AB

    PHENYTOIN

    Brand Name : PHENYTOIN

    Dosage Form : TABLET, CHEWABLE;ORAL

    Dosage Strength : 50MG

    Approval Date : 2014-04-17

    Application Number : 200565

    RX/OTC/DISCN : RX

    RLD : No

    TE Code : AB

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    07

    VIATRIS

    U.S.A
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    VIATRIS

    U.S.A
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    RLD : Yes

    TE Code : AB

    PHENYTOIN

    Brand Name : DILANTIN-125

    Dosage Form : SUSPENSION;ORAL

    Dosage Strength : 125MG/5ML

    Approval Date : 1982-01-01

    Application Number : 8762

    RX/OTC/DISCN : RX

    RLD : Yes

    TE Code : AB

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    08

    VIATRIS

    U.S.A
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    VIATRIS

    U.S.A
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    RLD : No

    TE Code :

    PHENYTOIN

    Brand Name : DILANTIN-30

    Dosage Form : SUSPENSION;ORAL

    Dosage Strength : 30MG/5ML

    Approval Date : 1982-01-01

    Application Number : 8762

    RX/OTC/DISCN : DISCN

    RLD : No

    TE Code :

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    09

    VISTAPHARM LLC

    India
    BioAsia
    Not Confirmed
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    VISTAPHARM LLC

    India
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    RLD : No

    TE Code :

    PHENYTOIN

    Brand Name : PHENYTOIN

    Dosage Form : SUSPENSION;ORAL

    Dosage Strength : 125MG/5ML

    Approval Date : 2001-01-31

    Application Number : 40342

    RX/OTC/DISCN : DISCN

    RLD : No

    TE Code :

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    10

    VISTAPHARM LLC

    India
    BioAsia
    Not Confirmed
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    VISTAPHARM LLC

    India
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    BioAsia
    Not Confirmed
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    RLD : No

    TE Code :

    PHENYTOIN

    Brand Name : PHENYTOIN

    Dosage Form : SUSPENSION;ORAL

    Dosage Strength : 125MG/5ML

    Approval Date : 2005-08-18

    Application Number : 40342

    RX/OTC/DISCN : DISCN

    RLD : No

    TE Code :

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