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    Graviti Pharmaceuticals

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    01 1ACETAMINOPHEN; TRAMADOL HYDROCHLORIDE

    02 4ATORVASTATIN CALCIUM

    03 2BACLOFEN

    04 2BUPROPION HYDROCHLORIDE

    05 3CYCLOBENZAPRINE HYDROCHLORIDE

    06 3ESCITALOPRAM OXALATE

    07 3ESOMEPRAZOLE MAGNESIUM

    08 2FAMOTIDINE

    09 3FUROSEMIDE

    10 3HYDROXYZINE HYDROCHLORIDE

    11 2TIZANIDINE HYDROCHLORIDE

    12 2TRAMADOL HYDROCHLORIDE

    13 4TRAZODONE HYDROCHLORIDE

    14 2VALACYCLOVIR HYDROCHLORIDE

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    Brand Name : TRAMADOL HYDROCHLORI...

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    Regulatory Info : DISCN

    Registration Country : USA

    ACETAMINOPHEN; TRAMADOL HYDROCHLORIDE

    Graviti Pharmaceuticals

    Dosage Form : TABLET;ORAL

    Brand Name : TRAMADOL HYDROCHLORIDE AN...

    Dosage Strength : 325MG;37.5MG

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    Approval Date : 2006-07-26

    Application Number : 76914

    Regulatory Info : DISCN

    Registration Country : USA

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    Regulatory Info : RX

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    ATORVASTATIN CALCIUM

    Graviti Pharmaceuticals

    Dosage Form : TABLET;ORAL

    Brand Name : ATORVASTATIN CALCIUM

    Dosage Strength : EQ 10MG BASE

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    Approval Date : 2018-06-18

    Application Number : 209912

    Regulatory Info : RX

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    Dosage Strength : EQ 20MG BASE

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    Approval Date : 2018-06-18

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    Dosage Strength : EQ 40MG BASE

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    Approval Date : 2018-06-18

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    Graviti Pharmaceuticals

    Dosage Form : TABLET;ORAL

    Brand Name : ATORVASTATIN CALCIUM

    Dosage Strength : EQ 80MG BASE

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    Approval Date : 2018-06-18

    Application Number : 209912

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    BACLOFEN

    Graviti Pharmaceuticals

    Dosage Form : TABLET;ORAL

    Brand Name : BACLOFEN

    Dosage Strength : 10MG

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    Approval Date : 2024-01-10

    Application Number : 217788

    Regulatory Info : RX

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    Dosage Form : TABLET;ORAL

    Brand Name : BACLOFEN

    Dosage Strength : 20MG

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    Approval Date : 2024-01-10

    Application Number : 217788

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    Dosage Form : TABLET, EXTENDED RELEASE...

    Brand Name : BUPROPION HYDROCHLORIDE

    Dosage Strength : 150MG

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    Approval Date : 2019-01-28

    Application Number : 211020

    Regulatory Info : RX

    Registration Country : USA

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    Dosage Form : TABLET, EXTENDED RELEASE...

    Brand Name : BUPROPION HYDROCHLORIDE

    Dosage Strength : 300MG

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    Approval Date : 2019-01-28

    Application Number : 211020

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    Brand Name : CYCLOBENZAPRINE HYDR...

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    Dosage Form : TABLET;ORAL

    Brand Name : CYCLOBENZAPRINE HYDROCHLO...

    Dosage Strength : 5MG

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    Approval Date : 2024-09-12

    Application Number : 218936

    Regulatory Info : RX

    Registration Country : USA

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