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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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    01 1ADAPALENE

    02 1CLOTRIMAZOLE

    03 1DIPHENHYDRAMINE HYDROCHLORIDE; NAPROXEN SODIUM

    04 1DOCOSANOL

    05 1ESOMEPRAZOLE MAGNESIUM

    06 1FAMOTIDINE

    07 3FEXOFENADINE HYDROCHLORIDE

    08 1IBUPROFEN

    09 1LORATADINE; PSEUDOEPHEDRINE SULFATE

    10 1MICONAZOLE NITRATE

    11 4MINOXIDIL

    12 30NICOTINE POLACRILEX

    13 1OMEPRAZOLE MAGNESIUM

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    01

    Brand Name : ADAPALENE

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

    U.S.A
    American Pharma Summit
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    RLD : No

    TE Code :

    ADAPALENE

    PL Developments

    Dosage Form : GEL; TOPICAL

    Proprietary Name : ADAPALENE

    Dosage Strength : 0.1%

    Approval Date : 2010-06-02

    Application Number : 90962

    RX/OTC/DISCN : OTC

    RLD : No

    TE Code :

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    02

    Brand Name : CLOTRIMAZOLE

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

    U.S.A
    American Pharma Summit
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    RLD : No

    TE Code :

    CLOTRIMAZOLE

    PL Developments

    Dosage Form : CREAM; VAGINAL

    Proprietary Name : CLOTRIMAZOLE

    Dosage Strength : 1%

    Approval Date : 1993-07-16

    Application Number : 74165

    RX/OTC/DISCN : OTC

    RLD : No

    TE Code :

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    03

    Brand Name : NAPROXEN SODIUM AND ...

    U.S.A
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    Brand Name : NAPROXEN SODIUM AND ...

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    RLD : No

    TE Code :

    DIPHENHYDRAMINE HYDROCHLORIDE; NAPROXEN SODIUM

    PL Developments

    Dosage Form : TABLET; ORAL

    Proprietary Name : NAPROXEN SODIUM AND DIPH...

    Dosage Strength : 25MG;220MG

    Approval Date : 2019-01-25

    Application Number : 207597

    RX/OTC/DISCN : DISCN

    RLD : No

    TE Code :

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    04

    Brand Name : DOCOSANOL

    U.S.A
    American Pharma Summit
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    Brand Name : DOCOSANOL

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    RLD : No

    TE Code :

    DOCOSANOL

    PL Developments

    Dosage Form : CREAM; TOPICAL

    Proprietary Name : DOCOSANOL

    Dosage Strength : 10%

    Approval Date : 2018-11-19

    Application Number : 208754

    RX/OTC/DISCN : OTC

    RLD : No

    TE Code :

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    05

    Brand Name : ESOMEPRAZOLE MAGNESI...

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

    U.S.A
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    RLD : No

    TE Code :

    ESOMEPRAZOLE MAGNESIUM

    PL Developments

    Dosage Form : TABLET, DELAYED RELEASE; ORAL

    Proprietary Name : ESOMEPRAZOLE MAGNESIUM

    Dosage Strength : EQ 20MG BASE

    Approval Date : 2019-03-05

    Application Number : 209202

    RX/OTC/DISCN : DISCN

    RLD : No

    TE Code :

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    Market
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    06

    Brand Name : FAMOTIDINE

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

    U.S.A
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    RLD : No

    TE Code :

    FAMOTIDINE

    PL Developments

    Dosage Form : TABLET; ORAL

    Proprietary Name : FAMOTIDINE

    Dosage Strength : 10MG

    Approval Date : 2001-07-26

    Application Number : 75512

    RX/OTC/DISCN : OTC

    RLD : No

    TE Code :

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    07

    Brand Name : FEXOFENADINE HYDROCH...

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

    U.S.A
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    RLD : No

    TE Code :

    FEXOFENADINE HYDROCHLORIDE

    PL Developments

    Dosage Form : SUSPENSION; ORAL

    Proprietary Name : FEXOFENADINE HYDROCHLORI...

    Dosage Strength : 30MG/5ML

    Approval Date : 2012-07-25

    Application Number : 201311

    RX/OTC/DISCN : DISCN

    RLD : No

    TE Code :

    blank

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    08

    Brand Name : CHILDRENS FEXOFENADI...

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

    U.S.A
    American Pharma Summit
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    RLD : No

    TE Code :

    FEXOFENADINE HYDROCHLORIDE

    PL Developments

    Dosage Form : SUSPENSION; ORAL

    Proprietary Name : CHILDRENS FEXOFENADINE H...

    Dosage Strength : 30MG/5ML

    Approval Date : 2014-11-18

    Application Number : 203330

    RX/OTC/DISCN : OTC

    RLD : No

    TE Code :

    blank

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    09

    Brand Name : CHILDRENS FEXOFENADI...

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

    U.S.A
    American Pharma Summit
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    RLD : No

    TE Code :

    FEXOFENADINE HYDROCHLORIDE

    PL Developments

    Dosage Form : SUSPENSION; ORAL

    Proprietary Name : CHILDRENS FEXOFENADINE H...

    Dosage Strength : 30MG/5ML

    Approval Date : 2014-11-18

    Application Number : 203330

    RX/OTC/DISCN : OTC

    RLD : No

    TE Code :

    blank

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    10

    Brand Name : IBUPROFEN

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

    U.S.A
    American Pharma Summit
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    RLD : No

    TE Code :

    IBUPROFEN

    PL Developments

    Dosage Form : SUSPENSION; ORAL

    Proprietary Name : IBUPROFEN

    Dosage Strength : 100MG/5ML

    Approval Date : 1999-04-30

    Application Number : 74916

    RX/OTC/DISCN : OTC

    RLD : No

    TE Code :

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