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    Granules India Limited has high volume world-class facilities for APIs, PFIs, & FDFs, serving customers in over 80 countries.

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    Jai Radhe Sales is your partner for all your sourcing needs.

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    Egis is a Hungarian generic pharma company with 110 years history. Our activities incorporate all areas of the pharma value chain.

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    Biophore is a research-driven global pharmaceutical company focused on niche APIs for the generic industry.

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    XGen Pharmaceuticals

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    FINISHED DOSAGE FORMULATIONS

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    01 1ACETAZOLAMIDE SODIUM

    02 1AMPHOTERICIN B

    03 1BACITRACIN

    04 1BACITRACIN ZINC

    05 2CLONIDINE HYDROCHLORIDE

    06 3CYCLOPHOSPHAMIDE

    07 1DACTINOMYCIN

    08 1FOLIC ACID

    09 1HYDROCORTISONE

    10 1HYDROCORTISONE ACETATE

    11 1IBUPROFEN LYSINE

    12 1LEVETIRACETAM

    13 1LINCOMYCIN HYDROCHLORIDE

    14 1LIOTHYRONINE SODIUM

    15 1NELARABINE

    16 2NEOMYCIN SULFATE

    17 2NEOMYCIN SULFATE; POLYMYXIN B SULFATE

    18 2PENTAMIDINE ISETHIONATE

    19 1POLYMYXIN B SULFATE

    20 2PROMETHAZINE HYDROCHLORIDE

    21 1STREPTOMYCIN SULFATE

    22 1TOBRAMYCIN SULFATE

    23 1TRANEXAMIC ACID

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    01

    Brand Name : ACETAZOLAMIDE SODIUM

    U.S.A
    American Pharma Summit
    Not Confirmed
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    Brand Name : ACETAZOLAMIDE SODIUM

    U.S.A
    American Pharma Summit
    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 : AMPHOTERICIN B

    U.S.A
    American Pharma Summit
    Not Confirmed
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    Brand Name : AMPHOTERICIN B

    U.S.A
    American Pharma Summit
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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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    03

    Brand Name : BACI-RX

    U.S.A
    American Pharma Summit
    Not Confirmed
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    Brand Name : BACI-RX

    U.S.A
    American Pharma Summit
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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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    04

    Brand Name : ZIBA-RX

    U.S.A
    American Pharma Summit
    Not Confirmed
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    Brand Name : ZIBA-RX

    U.S.A
    American Pharma Summit
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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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    05

    Brand Name : CLONIDINE HYDROCHLOR...

    U.S.A
    American Pharma Summit
    Not Confirmed
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    Brand Name : CLONIDINE HYDROCHLOR...

    U.S.A
    American Pharma Summit
    Not Confirmed
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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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    06

    Brand Name : CLONIDINE HYDROCHLOR...

    U.S.A
    American Pharma Summit
    Not Confirmed
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    Brand Name : CLONIDINE HYDROCHLOR...

    U.S.A
    American Pharma Summit
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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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    07

    Brand Name : CYCLOPHOSPHAMIDE

    U.S.A
    American Pharma Summit
    Not Confirmed
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    Brand Name : CYCLOPHOSPHAMIDE

    U.S.A
    American Pharma Summit
    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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    08

    Brand Name : CYCLOPHOSPHAMIDE

    U.S.A
    American Pharma Summit
    Not Confirmed
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    Brand Name : CYCLOPHOSPHAMIDE

    U.S.A
    American Pharma Summit
    Not Confirmed
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    • fda
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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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    09

    Brand Name : CYCLOPHOSPHAMIDE

    U.S.A
    American Pharma Summit
    Not Confirmed
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    Brand Name : CYCLOPHOSPHAMIDE

    U.S.A
    American Pharma Summit
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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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    10

    Brand Name : DACTINOMYCIN

    U.S.A
    American Pharma Summit
    Not Confirmed
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    Brand Name : DACTINOMYCIN

    U.S.A
    American Pharma Summit
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    RLD : No

    TE Code : AP

    DACTINOMYCIN

    XGen Pharmaceuticals

    Dosage Form : INJECTABLE; INJECTION

    Proprietary Name : DACTINOMYCIN

    Dosage Strength : 0.5MG/VIAL

    Approval Date : 2019-05-20

    Application Number : 203999

    RX/OTC/DISCN : RX

    RLD : No

    TE Code : AP

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