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

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    Metrochem has been delivering customized volume & quality products to customers across the world, taking utmost care of their needs.

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

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    Athena Pharmaceutiques is a Partner of Choice for Drug Delivery & Life Cycle Management.

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    XGen Pharmaceuticals

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    FINISHED DOSAGE FORMULATIONS

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    01 1ACETAZOLAMIDE SODIUM

    02 1ALCOHOL

    03 1AMPHOTERICIN B

    04 1BACITRACIN

    05 1BACITRACIN ZINC

    06 2CLONIDINE HYDROCHLORIDE

    07 3CYCLOPHOSPHAMIDE

    08 1DACTINOMYCIN

    09 2EDARAVONE

    10 1FOLIC ACID

    11 1HYDROCORTISONE

    12 1HYDROCORTISONE ACETATE

    13 1IBUPROFEN LYSINE

    14 1LEVETIRACETAM

    15 1LINCOMYCIN HYDROCHLORIDE

    16 1LIOTHYRONINE SODIUM

    17 1NELARABINE

    18 2NEOMYCIN SULFATE

    19 2NEOMYCIN SULFATE; POLYMYXIN B SULFATE

    20 2PENTAMIDINE ISETHIONATE

    21 1POLYMYXIN B SULFATE

    22 2PROMETHAZINE HYDROCHLORIDE

    23 1STREPTOMYCIN SULFATE

    24 1TOBRAMYCIN SULFATE

    25 1TRANEXAMIC ACID

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    01

    Brand Name : ACETAZOLAMIDE SODIUM

    U.S.A
    BIO Asia-Taiwan
    Not Confirmed
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    Brand Name : ACETAZOLAMIDE SODIUM

    U.S.A
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    BIO Asia-Taiwan
    Not Confirmed
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    Regulatory Info : RX

    Registration Country : USA

    ACETAZOLAMIDE SODIUM

    XGen Pharmaceuticals

    Dosage Form : INJECTABLE;INJECTION

    Brand Name : ACETAZOLAMIDE SODIUM

    Dosage Strength : EQ 500MG BASE/VIAL

    Packaging :

    Approval Date : 2008-12-10

    Application Number : 40784

    Regulatory Info : RX

    Registration Country : USA

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    02

    Brand Name : DEHYDRATED ALCOHOL

    U.S.A
    BIO Asia-Taiwan
    Not Confirmed
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    Brand Name : DEHYDRATED ALCOHOL

    U.S.A
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    BIO Asia-Taiwan
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    Regulatory Info :

    Registration Country : USA

    ALCOHOL

    XGen Pharmaceuticals

    Dosage Form : SOLUTION;INTRA-ARTERIAL

    Brand Name : DEHYDRATED ALCOHOL

    Dosage Strength : 99% (5ML)

    Packaging :

    Approval Date :

    Application Number : 219400

    Regulatory Info :

    Registration Country : USA

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    03

    Brand Name : AMPHOTERICIN B

    U.S.A
    BIO Asia-Taiwan
    Not Confirmed
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    Brand Name : AMPHOTERICIN B

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    Regulatory Info : RX

    Registration Country : USA

    AMPHOTERICIN B

    XGen Pharmaceuticals

    Dosage Form : INJECTABLE;INJECTION

    Brand Name : AMPHOTERICIN B

    Dosage Strength : 50MG/VIAL

    Packaging :

    Approval Date : 1992-04-29

    Application Number : 63206

    Regulatory Info : RX

    Registration Country : USA

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    04

    Brand Name : BACI-RX

    U.S.A
    BIO Asia-Taiwan
    Not Confirmed
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    Brand Name : BACI-RX

    U.S.A
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    Regulatory Info : DISCN

    Registration Country : USA

    BACITRACIN

    XGen Pharmaceuticals

    Dosage Form : POWDER;FOR RX COMPOUNDIN...

    Brand Name : BACI-RX

    Dosage Strength : 5,000,000 UNITS/BOT

    Packaging :

    Approval Date : 1982-01-01

    Application Number : 61580

    Regulatory Info : DISCN

    Registration Country : USA

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    05

    Brand Name : ZIBA-RX

    U.S.A
    BIO Asia-Taiwan
    Not Confirmed
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    Brand Name : ZIBA-RX

    U.S.A
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    Regulatory Info : DISCN

    Registration Country : USA

    BACITRACIN ZINC

    XGen Pharmaceuticals

    Dosage Form : POWDER;FOR RX COMPOUNDIN...

    Brand Name : ZIBA-RX

    Dosage Strength : 500,000 UNITS/BOT

    Packaging :

    Approval Date : 1982-01-01

    Application Number : 61737

    Regulatory Info : DISCN

    Registration Country : USA

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    06

    Brand Name : CLONIDINE HYDROCHLOR...

    U.S.A
    BIO Asia-Taiwan
    Not Confirmed
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    Brand Name : CLONIDINE HYDROCHLOR...

    U.S.A
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    BIO Asia-Taiwan
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    Regulatory Info : RX

    Registration Country : USA

    CLONIDINE HYDROCHLORIDE

    XGen Pharmaceuticals

    Dosage Form : INJECTABLE;INJECTION

    Brand Name : CLONIDINE HYDROCHLORIDE

    Dosage Strength : 1MG/10ML (0.1MG/ML)

    Packaging :

    Approval Date : 2013-10-29

    Application Number : 203167

    Regulatory Info : RX

    Registration Country : USA

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    07

    Brand Name : CLONIDINE HYDROCHLOR...

    U.S.A
    BIO Asia-Taiwan
    Not Confirmed
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    Brand Name : CLONIDINE HYDROCHLOR...

    U.S.A
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    BIO Asia-Taiwan
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    Regulatory Info : RX

    Registration Country : USA

    CLONIDINE HYDROCHLORIDE

    XGen Pharmaceuticals

    Dosage Form : INJECTABLE;INJECTION

    Brand Name : CLONIDINE HYDROCHLORIDE

    Dosage Strength : 5MG/10ML (0.5MG/ML)

    Packaging :

    Approval Date : 2013-10-29

    Application Number : 203167

    Regulatory Info : RX

    Registration Country : USA

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    08

    Brand Name : CYCLOPHOSPHAMIDE

    U.S.A
    BIO Asia-Taiwan
    Not Confirmed
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    Brand Name : CYCLOPHOSPHAMIDE

    U.S.A
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    BIO Asia-Taiwan
    Not Confirmed
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    Regulatory Info : RX

    Registration Country : USA

    CYCLOPHOSPHAMIDE

    XGen Pharmaceuticals

    Dosage Form : INJECTABLE;INJECTION

    Brand Name : CYCLOPHOSPHAMIDE

    Dosage Strength : 500MG/VIAL

    Packaging :

    Approval Date : 2022-10-18

    Application Number : 211757

    Regulatory Info : RX

    Registration Country : USA

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    09

    Brand Name : CYCLOPHOSPHAMIDE

    U.S.A
    BIO Asia-Taiwan
    Not Confirmed
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    Brand Name : CYCLOPHOSPHAMIDE

    U.S.A
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    Regulatory Info : RX

    Registration Country : USA

    CYCLOPHOSPHAMIDE

    XGen Pharmaceuticals

    Dosage Form : INJECTABLE;INJECTION

    Brand Name : CYCLOPHOSPHAMIDE

    Dosage Strength : 1GM/VIAL

    Packaging :

    Approval Date : 2022-10-18

    Application Number : 211757

    Regulatory Info : RX

    Registration Country : USA

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    10

    Brand Name : CYCLOPHOSPHAMIDE

    U.S.A
    BIO Asia-Taiwan
    Not Confirmed
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    Brand Name : CYCLOPHOSPHAMIDE

    U.S.A
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    Regulatory Info : RX

    Registration Country : USA

    CYCLOPHOSPHAMIDE

    XGen Pharmaceuticals

    Dosage Form : INJECTABLE;INJECTION

    Brand Name : CYCLOPHOSPHAMIDE

    Dosage Strength : 2GM/VIAL

    Packaging :

    Approval Date : 2022-10-18

    Application Number : 211757

    Regulatory Info : RX

    Registration Country : USA

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