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    Salix Pharmaceuticals's list of EU CTD Dossiers, Marketing Authorizations, In, Out Licensing Opportunities & Finished Dosage Formulations aggregated by PharmaCompass

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

    02 BUDESONIDE (2)

    03 CHLOROTHIAZIDE (1)

    04 FAMOTIDINE (1)

    05 FENOFIBRATE (2)

    06 HYDROCORTISONE (1)

    07 MAGNESIUM HYDROXIDE; OMEPRAZOLE; SODIUM BICARBONATE (4)

    08 MESALAMINE (1)

    09 METFORMIN HYDROCHLORIDE (2)

    10 METHYLNALTREXONE BROMIDE (5)

    11 METOCLOPRAMIDE HYDROCHLORIDE (2)

    12 OMEPRAZOLE; SODIUM BICARBONATE (5)

    13 PLECANATIDE (1)

    14 RIFAXIMIN (4)

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

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    01 SALIX (12)

    02 SALIX PHARMACEUTICALS INC (2)

    03 SALIX PHARMS (14)

    04 SANTARUS (5)

    05 SANTARUS INC (2)

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    01 AEROSOL, FOAM;RECTAL (1)

    02 CAPSULE, EXTENDED RELEASE;ORAL (1)

    03 CAPSULE;ORAL (2)

    04 CREAM;TOPICAL (1)

    05 FOR SOLUTION;ORAL (2)

    06 FOR SUSPENSION; ORAL (1)

    07 FOR SUSPENSION;ORAL (3)

    08 SOLUTION (1)

    09 SOLUTION;SUBCUTANEOUS (3)

    10 SUSPENSION;ORAL (1)

    11 TABLET (1)

    12 TABLET, CHEWABLE;ORAL (2)

    13 TABLET, EXTENDED RELEASE;ORAL (3)

    14 TABLET, ORALLY DISINTEGRATING;ORAL (2)

    15 TABLET;ORAL (11)

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    01 0.398GM;1.102GM (2)

    02 120MG (1)

    03 12MG/0.6ML (12MG/0.6ML) (2)

    04 150MG (1)

    05 1GM (1)

    06 2.5% (1)

    07 200MG (1)

    08 20MG/ML (1)

    09 20MG/PACKET;1.68GM/PACKET (1)

    10 20MG;1.1GM (1)

    11 250MG/5ML (1)

    12 2MG/ACTUATION (1)

    13 343MG;20MG;750MG (1)

    14 343MG;40MG;750MG (1)

    15 375MG (1)

    16 3MG (1)

    17 4.7GM;100GM;1.015GM;5.9GM;2.691GM;7.5GM (1)

    18 40MG (1)

    19 40MG/5ML **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons** (1)

    20 40MG/PACKET;1.68GM/PACKET (2)

    21 40MG;1.1GM (1)

    22 500MG (1)

    23 550MG (3)

    24 7.54GM;140GM;2.2GM;48.11GM;5.2GM;9GM (1)

    25 700MG;20MG;600MG (1)

    26 700MG;40MG;600MG (1)

    27 8MG/0.4ML (8MG/0.4ML) (1)

    28 9MG (1)

    29 EQ 10MG BASE **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons** (1)

    30 EQ 5MG BASE **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons** (1)

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    01 Canada (2)

    02 USA (33)

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

    PDF Supplier PDF
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    FOR SOLUTION;ORAL
    4.7GM;100GM;1.015GM;5....
    MOVIPREP
    USA
    21881
    2006-08-02
    RX
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    ASCORBIC ACID; POLYETHYLENE GLYCOL 3350; POTASSIUM CHLORIDE; SODIUM ASCORBATE; SODIUM CHLORIDE; SODIUM SULFATE

    PDF Supplier PDF
    URL Supplier Web Content
    FOR SOLUTION;ORAL
    7.54GM;140GM;2.2GM;48....
    PLENVU
    USA
    209381
    2018-05-04
    RX
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    BUDESONIDE

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    TABLET, EXTENDED RELEA...
    9MG
    UCERIS
    USA
    203634
    2013-01-14
    RX
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    BUDESONIDE

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    AEROSOL, FOAM;RECTAL
    2MG/ACTUATION
    UCERIS
    USA
    205613
    2014-10-07
    RX
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    CHLOROTHIAZIDE

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    SUSPENSION;ORAL
    250MG/5ML
    DIURIL
    USA
    11870
    1982-01-01
    RX
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    FAMOTIDINE

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    FOR SUSPENSION;ORAL
    40MG/5ML **Federal Reg...
    PEPCID
    USA
    19527
    1987-02-02
    DISCN
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    FENOFIBRATE

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    TABLET;ORAL
    40MG
    FENOGLIDE
    USA
    22118
    2007-08-10
    RX
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    FENOFIBRATE

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    TABLET;ORAL
    120MG
    FENOGLIDE
    USA
    22118
    2007-08-10
    RX
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    HYDROCORTISONE

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    CREAM;TOPICAL
    2.5%
    ANUSOL HC
    USA
    88250
    1984-06-06
    RX
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    MAGNESIUM HYDROXIDE; OMEPRAZOLE; SODIUM BICARBONATE

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    TABLET;ORAL
    343MG;40MG;750MG
    MAGNESIUM HYDROXIDE AN...
    USA
    22456
    2009-12-04
    DISCN
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