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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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    Salix Pharmaceuticals

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    01 2ASCORBIC ACID; POLYETHYLENE GLYCOL 3350; POTASSIUM CHLORIDE; SODIUM ASCORBATE; SODIUM CHLORIDE; SODIUM SULFATE

    02 2BUDESONIDE

    03 1CHLOROTHIAZIDE

    04 1FAMOTIDINE

    05 2FENOFIBRATE

    06 1HYDROCORTISONE

    07 4MAGNESIUM HYDROXIDE; OMEPRAZOLE; SODIUM BICARBONATE

    08 1MESALAMINE

    09 2METFORMIN HYDROCHLORIDE

    10 4METHYLNALTREXONE BROMIDE

    11 2METOCLOPRAMIDE HYDROCHLORIDE

    12 5OMEPRAZOLE; SODIUM BICARBONATE

    13 1PLECANATIDE

    14 3RIFAXIMIN

    15 2SODIUM PHOSPHATE, DIBASIC, ANHYDROUS; SODIUM PHOSPHATE, MONOBASIC, MONOHYDRATE

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    01

    Brand Name : MOVIPREP

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

    U.S.A
    Pharmtech & Ingredients
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    RLD : Yes

    TE Code : AA

    ASCORBIC ACID; POLYETHYLENE GLYCOL 3350; POTASSIUM CHLORIDE; SODIUM ASCORBATE; SODIUM CHLORIDE; SODIUM SULFATE

    Salix Pharmaceuticals

    Dosage Form : FOR SOLUTION; ORAL

    Proprietary Name : MOVIPREP

    Dosage Strength : 4.7GM;100GM;1.015GM;5.9G...

    Approval Date : 2006-08-02

    Application Number : 21881

    RX/OTC/DISCN : RX

    RLD : Yes

    TE Code : AA

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    02

    Brand Name : PLENVU

    U.S.A
    Pharmtech & Ingredients
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    Brand Name : PLENVU

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    RLD : Yes

    TE Code :

    ASCORBIC ACID; POLYETHYLENE GLYCOL 3350; POTASSIUM CHLORIDE; SODIUM ASCORBATE; SODIUM CHLORIDE; SODIUM SULFATE

    Salix Pharmaceuticals

    Dosage Form : FOR SOLUTION; ORAL

    Proprietary Name : PLENVU

    Dosage Strength : 7.54GM;140GM;2.2GM;48.11...

    Approval Date : 2018-05-04

    Application Number : 209381

    RX/OTC/DISCN : RX

    RLD : Yes

    TE Code :

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    03

    Brand Name : UCERIS

    U.S.A
    Pharmtech & Ingredients
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    Brand Name : UCERIS

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    RLD : Yes

    TE Code : AB

    BUDESONIDE

    Salix Pharmaceuticals

    Dosage Form : TABLET, EXTENDED RELEASE; ORAL

    Proprietary Name : UCERIS

    Dosage Strength : 9MG

    Approval Date : 2013-01-14

    Application Number : 203634

    RX/OTC/DISCN : RX

    RLD : Yes

    TE Code : AB

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    04

    Brand Name : UCERIS

    U.S.A
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    Brand Name : UCERIS

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    RLD : Yes

    TE Code : AB

    BUDESONIDE

    Salix Pharmaceuticals

    Dosage Form : AEROSOL, FOAM; RECTAL

    Proprietary Name : UCERIS

    Dosage Strength : 2MG/ACTUATION

    Approval Date : 2014-10-07

    Application Number : 205613

    RX/OTC/DISCN : RX

    RLD : Yes

    TE Code : AB

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    05

    Brand Name : DIURIL

    U.S.A
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    Brand Name : DIURIL

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    RLD : Yes

    TE Code :

    CHLOROTHIAZIDE

    Salix Pharmaceuticals

    Dosage Form : SUSPENSION; ORAL

    Proprietary Name : DIURIL

    Dosage Strength : 250MG/5ML

    Approval Date : 1982-01-01

    Application Number : 11870

    RX/OTC/DISCN : RX

    RLD : Yes

    TE Code :

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    06

    Brand Name : PEPCID

    U.S.A
    Pharmtech & Ingredients
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    Brand Name : PEPCID

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    RLD : Yes

    TE Code :

    FAMOTIDINE

    Salix Pharmaceuticals

    Dosage Form : FOR SUSPENSION; ORAL

    Proprietary Name : PEPCID

    Dosage Strength : 40MG/5ML **Federal Regis...

    Approval Date : 1987-02-02

    Application Number : 19527

    RX/OTC/DISCN : DISCN

    RLD : Yes

    TE Code :

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    07

    Brand Name : FENOGLIDE

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

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    RLD : Yes

    TE Code :

    FENOFIBRATE

    Salix Pharmaceuticals

    Dosage Form : TABLET; ORAL

    Proprietary Name : FENOGLIDE

    Dosage Strength : 40MG

    Approval Date : 2007-08-10

    Application Number : 22118

    RX/OTC/DISCN : DISCN

    RLD : Yes

    TE Code :

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    Brand Name : FENOGLIDE

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

    U.S.A
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    RLD : Yes

    TE Code :

    FENOFIBRATE

    Salix Pharmaceuticals

    Dosage Form : TABLET; ORAL

    Proprietary Name : FENOGLIDE

    Dosage Strength : 120MG

    Approval Date : 2007-08-10

    Application Number : 22118

    RX/OTC/DISCN : DISCN

    RLD : Yes

    TE Code :

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    09

    Brand Name : ANUSOL HC

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

    U.S.A
    Pharmtech & Ingredients
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    RLD : No

    TE Code : AT

    HYDROCORTISONE

    Salix Pharmaceuticals

    Dosage Form : CREAM; TOPICAL

    Proprietary Name : ANUSOL HC

    Dosage Strength : 2.5%

    Approval Date : 1984-06-06

    Application Number : 88250

    RX/OTC/DISCN : RX

    RLD : No

    TE Code : AT

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    10

    Brand Name : MAGNESIUM HYDROXIDE ...

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

    U.S.A
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    RLD : No

    TE Code :

    MAGNESIUM HYDROXIDE; OMEPRAZOLE; SODIUM BICARBONATE

    Salix Pharmaceuticals

    Dosage Form : TABLET; ORAL

    Proprietary Name : MAGNESIUM HYDROXIDE AND ...

    Dosage Strength : 343MG;20MG;750MG

    Approval Date : 2009-12-04

    Application Number : 22456

    RX/OTC/DISCN : DISCN

    RLD : No

    TE Code :

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