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    XGen Pharmaceuticals

    EVENTS

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    DIGITAL CONTENT

    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 1FOLIC ACID

    10 1HYDROCORTISONE

    11 1HYDROCORTISONE ACETATE

    12 1IBUPROFEN LYSINE

    13 1LEVETIRACETAM

    14 1LINCOMYCIN HYDROCHLORIDE

    15 1LIOTHYRONINE SODIUM

    16 1NELARABINE

    17 2NEOMYCIN SULFATE

    18 2NEOMYCIN SULFATE; POLYMYXIN B SULFATE

    19 1PENTAMIDINE ISETHIONATE

    20 1POLYMYXIN B SULFATE

    21 2PROMETHAZINE HYDROCHLORIDE

    22 1STREPTOMYCIN SULFATE

    23 1TOBRAMYCIN SULFATE

    24 1TRANEXAMIC ACID

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    01

    Brand Name : ACETAZOLAMIDE SODIUM

    U.S.A
    The MedTech Conference
    Not Confirmed
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    Brand Name : ACETAZOLAMIDE SODIUM

    U.S.A
    The MedTech Conference
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    RLD : No

    TE Code : AP

    ACETAZOLAMIDE SODIUM

    XGen Pharmaceuticals

    Dosage Form : INJECTABLE; INJECTION

    Proprietary Name : ACETAZOLAMIDE SODIUM

    Dosage Strength : EQ 500MG BASE/VIAL

    Approval Date : 2008-12-10

    Application Number : 40784

    RX/OTC/DISCN : RX

    RLD : No

    TE Code : AP

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    02

    Brand Name : DEHYDRATED ALCOHOL

    U.S.A
    The MedTech Conference
    Not Confirmed
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    Brand Name : DEHYDRATED ALCOHOL

    U.S.A
    The MedTech Conference
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    RLD : No

    TE Code : AP

    ALCOHOL

    XGen Pharmaceuticals

    Dosage Form : SOLUTION; INTRA-ARTERIAL

    Proprietary Name : DEHYDRATED ALCOHOL

    Dosage Strength : 99% (5ML)

    Approval Date : 2025-06-23

    Application Number : 219400

    RX/OTC/DISCN : RX

    RLD : No

    TE Code : AP

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    03

    Brand Name : AMPHOTERICIN B

    U.S.A
    The MedTech Conference
    Not Confirmed
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    Brand Name : AMPHOTERICIN B

    U.S.A
    The MedTech Conference
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    RLD : No

    TE Code :

    AMPHOTERICIN B

    XGen Pharmaceuticals

    Dosage Form : INJECTABLE; INJECTION

    Proprietary Name : AMPHOTERICIN B

    Dosage Strength : 50MG/VIAL

    Approval Date : 1992-04-29

    Application Number : 63206

    RX/OTC/DISCN : RX

    RLD : No

    TE Code :

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    04

    Brand Name : BACI-RX

    U.S.A
    The MedTech Conference
    Not Confirmed
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    Brand Name : BACI-RX

    U.S.A
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    RLD : No

    TE Code :

    BACITRACIN

    XGen Pharmaceuticals

    Dosage Form : POWDER; FOR RX COMPOUNDING

    Proprietary Name : BACI-RX

    Dosage Strength : 5,000,000 UNITS/BOT

    Approval Date : 1982-01-01

    Application Number : 61580

    RX/OTC/DISCN : DISCN

    RLD : No

    TE Code :

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    05

    Brand Name : ZIBA-RX

    U.S.A
    The MedTech Conference
    Not Confirmed
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    Brand Name : ZIBA-RX

    U.S.A
    The MedTech Conference
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    RLD : No

    TE Code :

    BACITRACIN ZINC

    XGen Pharmaceuticals

    Dosage Form : POWDER; FOR RX COMPOUNDING

    Proprietary Name : ZIBA-RX

    Dosage Strength : 500,000 UNITS/BOT

    Approval Date : 1982-01-01

    Application Number : 61737

    RX/OTC/DISCN : DISCN

    RLD : No

    TE Code :

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    06

    Brand Name : CLONIDINE HYDROCHLOR...

    U.S.A
    The MedTech Conference
    Not Confirmed
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    Brand Name : CLONIDINE HYDROCHLOR...

    U.S.A
    The MedTech Conference
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    RLD : No

    TE Code : AP

    CLONIDINE HYDROCHLORIDE

    XGen Pharmaceuticals

    Dosage Form : INJECTABLE; INJECTION

    Proprietary Name : CLONIDINE HYDROCHLORIDE

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

    Approval Date : 2013-10-29

    Application Number : 203167

    RX/OTC/DISCN : RX

    RLD : No

    TE Code : AP

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    07

    Brand Name : CLONIDINE HYDROCHLOR...

    U.S.A
    The MedTech Conference
    Not Confirmed
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    Brand Name : CLONIDINE HYDROCHLOR...

    U.S.A
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    RLD : No

    TE Code : AP

    CLONIDINE HYDROCHLORIDE

    XGen Pharmaceuticals

    Dosage Form : INJECTABLE; INJECTION

    Proprietary Name : CLONIDINE HYDROCHLORIDE

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

    Approval Date : 2013-10-29

    Application Number : 203167

    RX/OTC/DISCN : RX

    RLD : No

    TE Code : AP

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    08

    Brand Name : CYCLOPHOSPHAMIDE

    U.S.A
    The MedTech Conference
    Not Confirmed
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    Brand Name : CYCLOPHOSPHAMIDE

    U.S.A
    The MedTech Conference
    Not Confirmed
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    RLD : No

    TE Code : AP

    CYCLOPHOSPHAMIDE

    XGen Pharmaceuticals

    Dosage Form : INJECTABLE; INJECTION

    Proprietary Name : CYCLOPHOSPHAMIDE

    Dosage Strength : 500MG/VIAL

    Approval Date : 2022-10-18

    Application Number : 211757

    RX/OTC/DISCN : RX

    RLD : No

    TE Code : AP

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    09

    Brand Name : CYCLOPHOSPHAMIDE

    U.S.A
    The MedTech Conference
    Not Confirmed
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    Brand Name : CYCLOPHOSPHAMIDE

    U.S.A
    The MedTech Conference
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    RLD : No

    TE Code : AP

    CYCLOPHOSPHAMIDE

    XGen Pharmaceuticals

    Dosage Form : INJECTABLE; INJECTION

    Proprietary Name : CYCLOPHOSPHAMIDE

    Dosage Strength : 1GM/VIAL

    Approval Date : 2022-10-18

    Application Number : 211757

    RX/OTC/DISCN : RX

    RLD : No

    TE Code : AP

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    Brand Name : CYCLOPHOSPHAMIDE

    U.S.A
    The MedTech Conference
    Not Confirmed
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    Brand Name : CYCLOPHOSPHAMIDE

    U.S.A
    The MedTech Conference
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    RLD : No

    TE Code : AP

    CYCLOPHOSPHAMIDE

    XGen Pharmaceuticals

    Dosage Form : INJECTABLE; INJECTION

    Proprietary Name : CYCLOPHOSPHAMIDE

    Dosage Strength : 2GM/VIAL

    Approval Date : 2022-10-18

    Application Number : 211757

    RX/OTC/DISCN : RX

    RLD : No

    TE Code : AP

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