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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 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
    Fall Technical Meeting
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    Brand Name : ACETAZOLAMIDE SODIUM

    U.S.A
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    Fall Technical Meeting
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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
    Fall Technical Meeting
    Not Confirmed
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    Brand Name : DEHYDRATED ALCOHOL

    U.S.A
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    Fall Technical Meeting
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    Regulatory Info : RX

    Registration Country : USA

    ALCOHOL

    XGen Pharmaceuticals

    Dosage Form : SOLUTION;INTRA-ARTERIAL

    Brand Name : DEHYDRATED ALCOHOL

    Dosage Strength : 99% (5ML)

    Packaging :

    Approval Date : 2025-06-23

    Application Number : 219400

    Regulatory Info : RX

    Registration Country : USA

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    03

    Brand Name : AMPHOTERICIN B

    U.S.A
    Fall Technical Meeting
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    Brand Name : AMPHOTERICIN B

    U.S.A
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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
    Fall Technical Meeting
    Not Confirmed
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    Brand Name : BACI-RX

    U.S.A
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    Fall Technical Meeting
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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
    Fall Technical Meeting
    Not Confirmed
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    Brand Name : ZIBA-RX

    U.S.A
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    Fall Technical Meeting
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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
    Fall Technical Meeting
    Not Confirmed
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    Brand Name : CLONIDINE HYDROCHLOR...

    U.S.A
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    Fall Technical Meeting
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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
    Fall Technical Meeting
    Not Confirmed
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    Brand Name : CLONIDINE HYDROCHLOR...

    U.S.A
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    Fall Technical Meeting
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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
    Fall Technical Meeting
    Not Confirmed
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    Brand Name : CYCLOPHOSPHAMIDE

    U.S.A
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    Fall Technical Meeting
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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
    Fall Technical Meeting
    Not Confirmed
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    Brand Name : CYCLOPHOSPHAMIDE

    U.S.A
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    Fall Technical Meeting
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    Regulatory Info : RX

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    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
    Fall Technical Meeting
    Not Confirmed
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    Brand Name : CYCLOPHOSPHAMIDE

    U.S.A
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    Fall Technical Meeting
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    Regulatory Info : RX

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    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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