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    Slate Run Pharmaceuticals

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    FINISHED DOSAGE FORMULATIONS

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    01 1ACYCLOVIR SODIUM

    02 1AZITHROMYCIN

    03 1BIVALIRUDIN

    04 2CILOSTAZOL

    05 1DICYCLOMINE HYDROCHLORIDE

    06 1DOBUTAMINE HYDROCHLORIDE

    07 2DOXYCYCLINE HYCLATE

    08 2EPTIFIBATIDE

    09 1ESOMEPRAZOLE SODIUM

    10 1GANCICLOVIR SODIUM

    11 1LINCOMYCIN HYDROCHLORIDE

    12 1METHOCARBAMOL

    13 4SODIUM NITROPRUSSIDE

    14 1TOBRAMYCIN SULFATE

    15 4VANCOMYCIN HYDROCHLORIDE

    16 1VORICONAZOLE

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    01

    Brand Name : ACYCLOVIR SODIUM

    U.S.A
    DIA 2025
    Not Confirmed
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    Brand Name : ACYCLOVIR SODIUM

    U.S.A
    DIA 2025
    Not Confirmed
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    RLD : No

    TE Code : AP

    ACYCLOVIR SODIUM

    Slate Run Pharmaceuticals

    Dosage Form : INJECTABLE; INJECTION

    Proprietary Name : ACYCLOVIR SODIUM

    Dosage Strength : EQ 50MG BASE/ML

    Approval Date : 2024-01-08

    Application Number : 218111

    RX/OTC/DISCN : RX

    RLD : No

    TE Code : AP

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    02

    Brand Name : AZITHROMYCIN

    U.S.A
    DIA 2025
    Not Confirmed
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    Brand Name : AZITHROMYCIN

    U.S.A
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    RLD : No

    TE Code : AP

    AZITHROMYCIN

    Slate Run Pharmaceuticals

    Dosage Form : INJECTABLE; INJECTION

    Proprietary Name : AZITHROMYCIN

    Dosage Strength : EQ 500MG BASE/VIAL

    Approval Date : 2018-10-09

    Application Number : 203412

    RX/OTC/DISCN : RX

    RLD : No

    TE Code : AP

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    03

    Brand Name : BIVALIRUDIN

    U.S.A
    DIA 2025
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    Brand Name : BIVALIRUDIN

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    RLD : No

    TE Code : AP

    BIVALIRUDIN

    Slate Run Pharmaceuticals

    Dosage Form : INJECTABLE; INTRAVENOUS

    Proprietary Name : BIVALIRUDIN

    Dosage Strength : 250MG/VIAL

    Approval Date : 2021-05-28

    Application Number : 213078

    RX/OTC/DISCN : RX

    RLD : No

    TE Code : AP

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    04

    Brand Name : CILOSTAZOL

    U.S.A
    DIA 2025
    Not Confirmed
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    Brand Name : CILOSTAZOL

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    RLD : No

    TE Code : AB

    CILOSTAZOL

    Slate Run Pharmaceuticals

    Dosage Form : TABLET; ORAL

    Proprietary Name : CILOSTAZOL

    Dosage Strength : 100MG

    Approval Date : 2006-03-29

    Application Number : 77208

    RX/OTC/DISCN : RX

    RLD : No

    TE Code : AB

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    05

    Brand Name : CILOSTAZOL

    U.S.A
    DIA 2025
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    Brand Name : CILOSTAZOL

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    RLD : No

    TE Code : AB

    CILOSTAZOL

    Slate Run Pharmaceuticals

    Dosage Form : TABLET; ORAL

    Proprietary Name : CILOSTAZOL

    Dosage Strength : 50MG

    Approval Date : 2006-03-29

    Application Number : 77208

    RX/OTC/DISCN : RX

    RLD : No

    TE Code : AB

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    06

    Brand Name : DICYCLOMINE HYDROCHL...

    U.S.A
    DIA 2025
    Not Confirmed
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    Brand Name : DICYCLOMINE HYDROCHL...

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    RLD : No

    TE Code : AP

    DICYCLOMINE HYDROCHLORIDE

    Slate Run Pharmaceuticals

    Dosage Form : INJECTABLE; INJECTION

    Proprietary Name : DICYCLOMINE HYDROCHLORID...

    Dosage Strength : 10MG/ML

    Approval Date : 2018-11-02

    Application Number : 207076

    RX/OTC/DISCN : RX

    RLD : No

    TE Code : AP

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    07

    Brand Name : DOBUTAMINE HYDROCHLO...

    U.S.A
    DIA 2025
    Not Confirmed
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    Brand Name : DOBUTAMINE HYDROCHLO...

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    RLD : No

    TE Code : AP

    DOBUTAMINE HYDROCHLORIDE

    Slate Run Pharmaceuticals

    Dosage Form : INJECTABLE; INJECTION

    Proprietary Name : DOBUTAMINE HYDROCHLORIDE

    Dosage Strength : EQ 12.5MG BASE/ML

    Approval Date : 2022-12-21

    Application Number : 216131

    RX/OTC/DISCN : RX

    RLD : No

    TE Code : AP

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    08

    Brand Name : DOXYCYCLINE HYCLATE

    U.S.A
    DIA 2025
    Not Confirmed
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    Brand Name : DOXYCYCLINE HYCLATE

    U.S.A
    DIA 2025
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    RLD : No

    TE Code : AP

    DOXYCYCLINE HYCLATE

    Slate Run Pharmaceuticals

    Dosage Form : INJECTABLE; INJECTION

    Proprietary Name : DOXYCYCLINE HYCLATE

    Dosage Strength : EQ 100MG BASE/VIAL

    Approval Date : 2024-06-21

    Application Number : 217685

    RX/OTC/DISCN : RX

    RLD : No

    TE Code : AP

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    09

    Brand Name : DOXYCYCLINE HYCLATE

    U.S.A
    DIA 2025
    Not Confirmed
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    Brand Name : DOXYCYCLINE HYCLATE

    U.S.A
    DIA 2025
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    RLD : No

    TE Code : AP

    DOXYCYCLINE HYCLATE

    Slate Run Pharmaceuticals

    Dosage Form : INJECTABLE; INJECTION

    Proprietary Name : DOXYCYCLINE HYCLATE

    Dosage Strength : EQ 200MG BASE/VIAL

    Approval Date : 2024-06-21

    Application Number : 217685

    RX/OTC/DISCN : RX

    RLD : No

    TE Code : AP

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    10

    Brand Name : EPTIFIBATIDE

    U.S.A
    DIA 2025
    Not Confirmed
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    Brand Name : EPTIFIBATIDE

    U.S.A
    DIA 2025
    Not Confirmed
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    RLD : No

    TE Code : AP

    EPTIFIBATIDE

    Slate Run Pharmaceuticals

    Dosage Form : INJECTABLE; INJECTION

    Proprietary Name : EPTIFIBATIDE

    Dosage Strength : 2MG/ML

    Approval Date : 2019-01-25

    Application Number : 209864

    RX/OTC/DISCN : RX

    RLD : No

    TE Code : AP

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