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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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    Bayshore Pharmaceuticals

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    FINISHED DOSAGE FORMULATIONS

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    01 1ATROPINE SULFATE; DIPHENOXYLATE HYDROCHLORIDE

    02 5ETODOLAC

    03 1KETOTIFEN FUMARATE

    04 2METHSCOPOLAMINE BROMIDE

    05 3METOLAZONE

    06 1ORPHENADRINE CITRATE

    07 2PINDOLOL

    08 1PRIMAQUINE PHOSPHATE

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    01

    Brand Name : DIPHENOXYLATE HYDROC...

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    Brand Name : DIPHENOXYLATE HYDROC...

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    RLD : No

    TE Code : AA

    ATROPINE SULFATE; DIPHENOXYLATE HYDROCHLORIDE

    Bayshore Pharmaceuticals

    Dosage Form : TABLET; ORAL

    Proprietary Name : DIPHENOXYLATE HYDROCHLOR...

    Dosage Strength : 0.025MG;2.5MG

    Approval Date : 2018-11-13

    Application Number : 210819

    RX/OTC/DISCN : RX

    RLD : No

    TE Code : AA

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    02

    Brand Name : ETODOLAC

    U.S.A
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    Brand Name : ETODOLAC

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    RLD : No

    TE Code : AB

    ETODOLAC

    Bayshore Pharmaceuticals

    Dosage Form : TABLET; ORAL

    Proprietary Name : ETODOLAC

    Dosage Strength : 400MG

    Approval Date : 2020-12-16

    Application Number : 210704

    RX/OTC/DISCN : RX

    RLD : No

    TE Code : AB

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    03

    Brand Name : ETODOLAC

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    RLD : No

    TE Code : AB

    ETODOLAC

    Bayshore Pharmaceuticals

    Dosage Form : TABLET; ORAL

    Proprietary Name : ETODOLAC

    Dosage Strength : 500MG

    Approval Date : 2020-12-16

    Application Number : 210704

    RX/OTC/DISCN : RX

    RLD : No

    TE Code : AB

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    04

    Brand Name : ETODOLAC

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    RLD : No

    TE Code : AB

    ETODOLAC

    Bayshore Pharmaceuticals

    Dosage Form : TABLET, EXTENDED RELEASE; ORAL

    Proprietary Name : ETODOLAC

    Dosage Strength : 400MG

    Approval Date : 2020-11-24

    Application Number : 212263

    RX/OTC/DISCN : RX

    RLD : No

    TE Code : AB

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    05

    Brand Name : ETODOLAC

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    RLD : No

    TE Code : AB

    ETODOLAC

    Bayshore Pharmaceuticals

    Dosage Form : TABLET, EXTENDED RELEASE; ORAL

    Proprietary Name : ETODOLAC

    Dosage Strength : 500MG

    Approval Date : 2020-11-24

    Application Number : 212263

    RX/OTC/DISCN : RX

    RLD : No

    TE Code : AB

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    06

    Brand Name : ETODOLAC

    U.S.A
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    Brand Name : ETODOLAC

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    RLD : No

    TE Code : AB

    ETODOLAC

    Bayshore Pharmaceuticals

    Dosage Form : TABLET, EXTENDED RELEASE; ORAL

    Proprietary Name : ETODOLAC

    Dosage Strength : 600MG

    Approval Date : 2020-11-24

    Application Number : 212263

    RX/OTC/DISCN : RX

    RLD : No

    TE Code : AB

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    07

    Brand Name : KETOTIFEN FUMARATE

    U.S.A
    Pharmtech & Ingredients
    Not Confirmed
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    Brand Name : KETOTIFEN FUMARATE

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    Pharmtech & Ingredients
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    RLD : No

    TE Code :

    KETOTIFEN FUMARATE

    Bayshore Pharmaceuticals

    Dosage Form : SOLUTION/DROPS; OPHTHALMIC

    Proprietary Name : KETOTIFEN FUMARATE

    Dosage Strength : EQ 0.025% BASE

    Approval Date : 2020-06-01

    Application Number : 204059

    RX/OTC/DISCN : OTC

    RLD : No

    TE Code :

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    08

    Brand Name : METHSCOPOLAMINE BROM...

    U.S.A
    Pharmtech & Ingredients
    Not Confirmed
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    Brand Name : METHSCOPOLAMINE BROM...

    U.S.A
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    RLD : No

    TE Code : AA

    METHSCOPOLAMINE BROMIDE

    Bayshore Pharmaceuticals

    Dosage Form : TABLET; ORAL

    Proprietary Name : METHSCOPOLAMINE BROMIDE

    Dosage Strength : 2.5MG

    Approval Date : 2012-09-24

    Application Number : 200602

    RX/OTC/DISCN : RX

    RLD : No

    TE Code : AA

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    09

    Brand Name : METHSCOPOLAMINE BROM...

    U.S.A
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    Not Confirmed
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    Brand Name : METHSCOPOLAMINE BROM...

    U.S.A
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    RLD : No

    TE Code : AA

    METHSCOPOLAMINE BROMIDE

    Bayshore Pharmaceuticals

    Dosage Form : TABLET; ORAL

    Proprietary Name : METHSCOPOLAMINE BROMIDE

    Dosage Strength : 5MG

    Approval Date : 2012-09-24

    Application Number : 200602

    RX/OTC/DISCN : RX

    RLD : No

    TE Code : AA

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    10

    Brand Name : METOLAZONE

    U.S.A
    Pharmtech & Ingredients
    Not Confirmed
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    Brand Name : METOLAZONE

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    RLD : No

    TE Code : AB

    METOLAZONE

    Bayshore Pharmaceuticals

    Dosage Form : TABLET; ORAL

    Proprietary Name : METOLAZONE

    Dosage Strength : 2.5MG

    Approval Date : 2021-03-30

    Application Number : 214799

    RX/OTC/DISCN : RX

    RLD : No

    TE Code : AB

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