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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
    Pharmex
    Not Confirmed
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    Brand Name : ACETAZOLAMIDE SODIUM

    U.S.A
    Pharmex
    Not Confirmed
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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
    Pharmex
    Not Confirmed
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    Brand Name : DEHYDRATED ALCOHOL

    U.S.A
    Pharmex
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    RLD :

    TE Code :

    ALCOHOL

    XGen Pharmaceuticals

    Dosage Form : SOLUTION; INTRA-ARTERIAL

    Proprietary Name : DEHYDRATED ALCOHOL

    Dosage Strength : 99% (5ML)

    Approval Date :

    Application Number : 219400

    RX/OTC/DISCN :

    RLD :

    TE Code :

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    03

    Brand Name : AMPHOTERICIN B

    U.S.A
    Pharmex
    Not Confirmed
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    Brand Name : AMPHOTERICIN B

    U.S.A
    Pharmex
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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
    Pharmex
    Not Confirmed
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    Brand Name : BACI-RX

    U.S.A
    Pharmex
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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
    Pharmex
    Not Confirmed
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    Brand Name : ZIBA-RX

    U.S.A
    Pharmex
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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
    Pharmex
    Not Confirmed
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    Brand Name : CLONIDINE HYDROCHLOR...

    U.S.A
    Pharmex
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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
    Pharmex
    Not Confirmed
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    Brand Name : CLONIDINE HYDROCHLOR...

    U.S.A
    Pharmex
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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
    Pharmex
    Not Confirmed
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    Brand Name : CYCLOPHOSPHAMIDE

    U.S.A
    Pharmex
    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
    Pharmex
    Not Confirmed
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    Brand Name : CYCLOPHOSPHAMIDE

    U.S.A
    Pharmex
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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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    10

    Brand Name : CYCLOPHOSPHAMIDE

    U.S.A
    Pharmex
    Not Confirmed
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    Brand Name : CYCLOPHOSPHAMIDE

    U.S.A
    Pharmex
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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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