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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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    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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    01 2BUPROPION HYDROCHLORIDE

    02 3FLUOXETINE HYDROCHLORIDE

    03 2MECLIZINE HYDROCHLORIDE

    04 4PRAVASTATIN SODIUM

    05 4TERAZOSIN HYDROCHLORIDE

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    Brand Name : BUPROPION HYDROCHLOR...

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    CPhI India 2024
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    Brand Name : BUPROPION HYDROCHLOR...

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    BUPROPION HYDROCHLORIDE

    Apnar Pharma

    Dosage Form : TABLET;ORAL

    Brand Name : BUPROPION HYDROCHLORIDE

    Dosage Strength : 75MG

    Packaging :

    Approval Date : 2000-02-07

    Application Number : 75584

    Regulatory Info : RX

    Registration Country : USA

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    Brand Name : BUPROPION HYDROCHLOR...

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    Brand Name : BUPROPION HYDROCHLOR...

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    BUPROPION HYDROCHLORIDE

    Apnar Pharma

    Dosage Form : TABLET;ORAL

    Brand Name : BUPROPION HYDROCHLORIDE

    Dosage Strength : 100MG

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    Approval Date : 2000-02-07

    Application Number : 75584

    Regulatory Info : RX

    Registration Country : USA

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    03

    Brand Name : FLUOXETINE HYDROCHLO...

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    FLUOXETINE HYDROCHLORIDE

    Apnar Pharma

    Dosage Form : CAPSULE;ORAL

    Brand Name : FLUOXETINE HYDROCHLORIDE

    Dosage Strength : EQ 10MG BASE

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    Approval Date : 2001-08-02

    Application Number : 75049

    Regulatory Info : RX

    Registration Country : USA

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    Brand Name : FLUOXETINE HYDROCHLO...

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    Regulatory Info : RX

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    FLUOXETINE HYDROCHLORIDE

    Apnar Pharma

    Dosage Form : CAPSULE;ORAL

    Brand Name : FLUOXETINE HYDROCHLORIDE

    Dosage Strength : EQ 20MG BASE

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    Approval Date : 2002-01-29

    Application Number : 75049

    Regulatory Info : RX

    Registration Country : USA

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    Brand Name : FLUOXETINE HYDROCHLO...

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    CPhI India 2024
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    FLUOXETINE HYDROCHLORIDE

    Apnar Pharma

    Dosage Form : CAPSULE;ORAL

    Brand Name : FLUOXETINE HYDROCHLORIDE

    Dosage Strength : EQ 40MG BASE

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    Approval Date : 2002-01-29

    Application Number : 75049

    Regulatory Info : RX

    Registration Country : USA

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    06

    Brand Name : MECLIZINE HYDROCHLOR...

    U.S.A
    CPhI India 2024
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    Brand Name : MECLIZINE HYDROCHLOR...

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    Regulatory Info : RX

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    MECLIZINE HYDROCHLORIDE

    Apnar Pharma

    Dosage Form : TABLET;ORAL

    Brand Name : MECLIZINE HYDROCHLORIDE

    Dosage Strength : 25MG

    Packaging :

    Approval Date : 1982-01-01

    Application Number : 87128

    Regulatory Info : RX

    Registration Country : USA

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    Brand Name : MECLIZINE HYDROCHLOR...

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    Brand Name : MECLIZINE HYDROCHLOR...

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    Regulatory Info : RX

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    MECLIZINE HYDROCHLORIDE

    Apnar Pharma

    Dosage Form : TABLET;ORAL

    Brand Name : MECLIZINE HYDROCHLORIDE

    Dosage Strength : 12.5MG

    Packaging :

    Approval Date : 1982-01-01

    Application Number : 87128

    Regulatory Info : RX

    Registration Country : USA

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    08

    Brand Name : PRAVASTATIN SODIUM

    U.S.A
    CPhI India 2024
    Not Confirmed
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    Brand Name : PRAVASTATIN SODIUM

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    Regulatory Info : RX

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    PRAVASTATIN SODIUM

    Apnar Pharma

    Dosage Form : TABLET;ORAL

    Brand Name : PRAVASTATIN SODIUM

    Dosage Strength : 80MG

    Packaging :

    Approval Date : 2008-02-11

    Application Number : 77491

    Regulatory Info : RX

    Registration Country : USA

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    Brand Name : PRAVASTATIN SODIUM

    U.S.A
    CPhI India 2024
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    Brand Name : PRAVASTATIN SODIUM

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    PRAVASTATIN SODIUM

    Apnar Pharma

    Dosage Form : TABLET;ORAL

    Brand Name : PRAVASTATIN SODIUM

    Dosage Strength : 10MG

    Packaging :

    Approval Date : 2006-10-23

    Application Number : 77491

    Regulatory Info : RX

    Registration Country : USA

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    Brand Name : PRAVASTATIN SODIUM

    U.S.A
    CPhI India 2024
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    Brand Name : PRAVASTATIN SODIUM

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    PRAVASTATIN SODIUM

    Apnar Pharma

    Dosage Form : TABLET;ORAL

    Brand Name : PRAVASTATIN SODIUM

    Dosage Strength : 40MG

    Packaging :

    Approval Date : 2006-10-23

    Application Number : 77491

    Regulatory Info : RX

    Registration Country : USA

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