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    EUROAPI, the leading small molecules API player, provides both API sales & CDMO services.

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    Interquim comes from an international group of 50 companies active in the pharma, hospital, diagnostics, fine chemicals & feed sectors.

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    03 1ANGITA PHARMA INC.

    04 1Alcon Inc

    05 1Aralez Pharmaceuticals

    06 1Aurobindo Pharma Limited

    07 7BRAINTREE LABS

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    09 1CellChem Pharmaceuticals

    10 1Dynapharm

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    01

    Strides Pharma Science

    India
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    Virtual BoothStrides Pharma Science: Pioneering IP-driven formulations for niche finished dosage forms.

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    POLYETHYLENE GLYCOL 3350; POTASSIUM CHLORIDE; SODIUM BICARBONATE; SODIUM CHLORIDE; SODIUM SULFATE ANHYDROUS

    Brand Name : POLYETHYLENE GLYCOL 3350 AND ELECTROLYTES

    Dosage Form : FOR SOLUTION;ORAL

    Dosage Strength : 236GM/BOT;2.97GM/BOT;6.74GM/BOT;5.86GM/BOT;22.74GM/BOT

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    Approval Date : 2018-12-21

    Application Number : 204558

    Regulatory Info : RX

    Registration Country : USA

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    TAPI Technology & API Services

    Israel
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    Virtual BoothTAPI, a leading global supplier of APIs, provides over 350 products and customized CDMO solutions for every stage of development.

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    Regulatory Info : DISCN

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    POLYETHYLENE GLYCOL 3350; POTASSIUM CHLORIDE; SODIUM BICARBONATE; SODIUM CHLORIDE; SODIUM SULFATE ANHYDROUS

    Brand Name : GLYCOPREP

    Dosage Form : FOR SUSPENSION;ORAL

    Dosage Strength : 236GM/BOT;2.97GM/BOT;6.74GM/BOT;5.86GM/BOT;22.74GM/BOT

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    Approval Date : 1988-12-23

    Application Number : 72319

    Regulatory Info : DISCN

    Registration Country : USA

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    03

    Strides Pharma Science

    India
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    POLYETHYLENE GLYCOL 3350; POTASSIUM CHLORIDE; SODIUM BICARBONATE; SODIUM CHLORIDE

    Brand Name : PEG-3350, POTASSIUM CHLORIDE, SODIUM BICARBONATE, SODIUM CHLORIDE

    Dosage Form : FOR SOLUTION;ORAL

    Dosage Strength : 420GM/BOT;1.48GM/BOT;5.72GM/BOT;11.2GM/BOT

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    Approval Date : 2015-04-13

    Application Number : 204559

    Regulatory Info : RX

    Registration Country : USA

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    04

    Aurobindo Pharma Limited

    India
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    Aurobindo Pharma Limited

    India
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    Regulatory Info : DISCN

    Registration Country : USA

    POLYETHYLENE GLYCOL 3350; POTASSIUM CHLORIDE; SODIUM BICARBONATE; SODIUM CHLORIDE

    Brand Name : TRILYTE

    Dosage Form : FOR SOLUTION;ORAL

    Dosage Strength : 420GM/BOT;1.48GM/BOT;5.72GM/BOT;11.2GM/BOT

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    Approval Date : 2004-02-05

    Application Number : 76491

    Regulatory Info : DISCN

    Registration Country : USA

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    05

    BRAINTREE LABS

    U.S.A
    The Generic Rx Session
    Not Confirmed
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    BRAINTREE LABS

    U.S.A
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    Regulatory Info : RX

    Registration Country : USA

    POLYETHYLENE GLYCOL 3350; POTASSIUM CHLORIDE; SODIUM BICARBONATE; SODIUM CHLORIDE; SODIUM SULFATE ANHYDROUS

    Brand Name : GOLYTELY

    Dosage Form : FOR SOLUTION;ORAL

    Dosage Strength : 236GM/BOT;2.97GM/BOT;6.74GM/BOT;5.86GM/BOT;22.74GM/BOT

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    Approval Date : 1984-07-13

    Application Number : 19011

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    Registration Country : USA

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    06

    BRAINTREE LABS

    U.S.A
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    BRAINTREE LABS

    U.S.A
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    Regulatory Info : DISCN

    Registration Country : USA

    POLYETHYLENE GLYCOL 3350; POTASSIUM CHLORIDE; SODIUM BICARBONATE; SODIUM CHLORIDE; SODIUM SULFATE ANHYDROUS

    Brand Name : GOLYTELY

    Dosage Form : FOR SOLUTION;ORAL

    Dosage Strength : 227.1GM/PACKET;2.82GM/PACKET;6.36GM/PACKET;5.53GM/PACKET;21.5GM/PACKET

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    Approval Date : 1992-06-02

    Application Number : 19011

    Regulatory Info : DISCN

    Registration Country : USA

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    07

    BRAINTREE LABS

    U.S.A
    The Generic Rx Session
    Not Confirmed
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    BRAINTREE LABS

    U.S.A
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    Regulatory Info : RX

    Registration Country : USA

    POLYETHYLENE GLYCOL 3350; POTASSIUM CHLORIDE; SODIUM BICARBONATE; SODIUM CHLORIDE

    Brand Name : NULYTELY

    Dosage Form : FOR SOLUTION;ORAL

    Dosage Strength : 420GM/BOT;1.48GM/BOT;5.72GM/BOT;11.2GM/BOT

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    Approval Date : 1991-04-22

    Application Number : 19797

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    Registration Country : USA

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    08

    BRAINTREE LABS

    U.S.A
    The Generic Rx Session
    Not Confirmed
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    BRAINTREE LABS

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    Regulatory Info : RX

    Registration Country : USA

    POLYETHYLENE GLYCOL 3350; POTASSIUM CHLORIDE; SODIUM BICARBONATE; SODIUM CHLORIDE

    Brand Name : NULYTELY-FLAVORED

    Dosage Form : FOR SOLUTION;ORAL

    Dosage Strength : 420GM/BOT;1.48GM/BOT;5.72GM/BOT;11.2GM/BOT

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    Approval Date : 1994-11-18

    Application Number : 19797

    Regulatory Info : RX

    Registration Country : USA

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    09

    BRAINTREE LABS

    U.S.A
    The Generic Rx Session
    Not Confirmed
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    BRAINTREE LABS

    U.S.A
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    The Generic Rx Session
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    Regulatory Info :

    Registration Country : USA

    BISACODYL; POLYETHYLENE GLYCOL 3350; POTASSIUM CHLORIDE; SODIUM BICARBONATE; SODIUM CHLORIDE

    Brand Name : HALFLYTELY

    Dosage Form : FOR SOLUTION, TABLET, DELAYED RELEASE;ORAL

    Dosage Strength : 5MG,N/A;N/A,210GM;N/A,0.74GM;N/A,2.86GM;N/A,5.6GM

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    Approval Date :

    Application Number : 21551

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    Registration Country : USA

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    10

    BRAINTREE LABS

    U.S.A
    The Generic Rx Session
    Not Confirmed
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    BRAINTREE LABS

    U.S.A
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    The Generic Rx Session
    Not Confirmed
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    Regulatory Info : DISCN

    Registration Country : USA

    BISACODYL; POLYETHYLENE GLYCOL 3350; POTASSIUM CHLORIDE; SODIUM BICARBONATE; SODIUM CHLORIDE

    Brand Name : HALFLYTELY

    Dosage Form : FOR SOLUTION, TABLET, DELAYED RELEASE;ORAL

    Dosage Strength : 5MG,N/A;N/A,210GM;N/A,0.74GM;N/A,2.86GM;N/A,5.6GM **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons**

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    Approval Date : 2010-07-16

    Application Number : 21551

    Regulatory Info : DISCN

    Registration Country : USA

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    11

    Dynapharm

    Malaysia
    The Generic Rx Session
    Not Confirmed
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    Dynapharm

    Malaysia
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    The Generic Rx Session
    Not Confirmed
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    Regulatory Info : DISCN

    Registration Country : USA

    POLYETHYLENE GLYCOL 3350; POTASSIUM CHLORIDE; SODIUM BICARBONATE; SODIUM CHLORIDE; SODIUM SULFATE ANHYDROUS

    Brand Name : COLOVAGE

    Dosage Form : FOR SUSPENSION;ORAL

    Dosage Strength : 227.1GM/PACKET;2.82GM/PACKET;6.36GM/PACKET;5.53GM/PACKET;21.5GM/PACKET

    Packaging :

    Approval Date : 1988-04-20

    Application Number : 71320

    Regulatory Info : DISCN

    Registration Country : USA

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    12

    E-Z-EM Canada Inc, dba Therapex

    Canada
    The Generic Rx Session
    Not Confirmed
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    E-Z-EM Canada Inc, dba Therapex

    Canada
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    The Generic Rx Session
    Not Confirmed
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    Regulatory Info : DISCN

    Registration Country : USA

    POLYETHYLENE GLYCOL 3350; POTASSIUM CHLORIDE; SODIUM BICARBONATE; SODIUM CHLORIDE; SODIUM SULFATE ANHYDROUS

    Brand Name : E-Z-EM PREP LYTE

    Dosage Form : FOR SUSPENSION;ORAL

    Dosage Strength : 236GM/BOT;2.97GM/BOT;6.74GM/BOT;5.86GM/BOT;22.74GM/BOT

    Packaging :

    Approval Date : 1988-11-21

    Application Number : 71278

    Regulatory Info : DISCN

    Registration Country : USA

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    13

    Hospira, Inc.

    U.S.A
    The Generic Rx Session
    Not Confirmed
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    Hospira, Inc.

    U.S.A
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    The Generic Rx Session
    Not Confirmed
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    Regulatory Info : DISCN

    Registration Country : USA

    POLYETHYLENE GLYCOL 3350; POTASSIUM CHLORIDE; SODIUM BICARBONATE; SODIUM CHLORIDE; SODIUM SULFATE

    Brand Name : OCL

    Dosage Form : SOLUTION;ORAL

    Dosage Strength : 6GM/100ML;75MG/100ML;168MG/100ML;146MG/100ML;1.29GM/100ML

    Packaging :

    Approval Date : 1986-04-30

    Application Number : 19284

    Regulatory Info : DISCN

    Registration Country : USA

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    14

    Novel Laboratories, Inc.

    U.S.A
    The Generic Rx Session
    Not Confirmed
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    Novel Laboratories, Inc.

    U.S.A
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    Regulatory Info : RX

    Registration Country : USA

    POLYETHYLENE GLYCOL 3350; POTASSIUM CHLORIDE; SODIUM BICARBONATE; SODIUM CHLORIDE

    Brand Name : PEG-3350, POTASSIUM CHLORIDE, SODIUM BICARBONATE, SODIUM CHLORIDE

    Dosage Form : FOR SOLUTION;ORAL

    Dosage Strength : 420GM/BOT;1.48GM/BOT;5.72GM/BOT;11.2GM/BOT

    Packaging :

    Approval Date : 2009-05-27

    Application Number : 90019

    Regulatory Info : RX

    Registration Country : USA

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    15

    Novel Laboratories, Inc.

    U.S.A
    The Generic Rx Session
    Not Confirmed
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    Novel Laboratories, Inc.

    U.S.A
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    Regulatory Info : RX

    Registration Country : USA

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

    Brand Name : PEG-3350, SODIUM SULFATE, SODIUM CHLORIDE, POTASSIUM CHLORIDE, SODIUM ASCORBATE AND ASCORBIC ACID

    Dosage Form : FOR SOLUTION;ORAL

    Dosage Strength : 4.7GM;100GM;1.015GM;5.9GM;2.691GM;7.5GM

    Packaging :

    Approval Date : 2012-01-25

    Application Number : 90145

    Regulatory Info : RX

    Registration Country : USA

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    16

    Novel Laboratories, Inc.

    U.S.A
    The Generic Rx Session
    Not Confirmed
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    Novel Laboratories, Inc.

    U.S.A
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    The Generic Rx Session
    Not Confirmed
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    Regulatory Info : RX

    Registration Country : USA

    POLYETHYLENE GLYCOL 3350; POTASSIUM CHLORIDE; SODIUM BICARBONATE; SODIUM CHLORIDE; SODIUM SULFATE ANHYDROUS

    Brand Name : PEG 3350 AND ELECTROLYTES

    Dosage Form : FOR SOLUTION;ORAL

    Dosage Strength : 240GM/BOT;2.98GM/BOT;6.72GM/BOT;5.84GM/BOT;22.72GM/BOT

    Packaging :

    Approval Date : 2009-06-01

    Application Number : 90186

    Regulatory Info : RX

    Registration Country : USA

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    17

    Novel Laboratories, Inc.

    U.S.A
    The Generic Rx Session
    Not Confirmed
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    Novel Laboratories, Inc.

    U.S.A
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    The Generic Rx Session
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    Regulatory Info :

    Registration Country : USA

    POLYETHYLENE GLYCOL 3350; SODIUM CHLORIDE; SODIUM BICARBONATE; POTASSIUM CHLORIDE; BISACODYL

    Brand Name : POLYETHYLENE GLYCOL 3350; SODIUM CHLORIDE; SODIUM BICARBONATE; POTASSIUM CHLORIDE; BISACODYL

    Dosage Form : SOLUTION; ORAL AND TABLET; DELAYED RELEASE

    Dosage Strength : 2MG; 5MG

    Packaging :

    Approval Date :

    Application Number : 90197

    Regulatory Info :

    Registration Country : USA

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    18

    Perrigo Company plc

    Ireland
    The Generic Rx Session
    Not Confirmed
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    Perrigo Company plc

    Ireland
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    The Generic Rx Session
    Not Confirmed
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    Regulatory Info : DISCN

    Registration Country : USA

    POLYETHYLENE GLYCOL 3350; POTASSIUM CHLORIDE; SODIUM BICARBONATE; SODIUM CHLORIDE

    Brand Name : LAX-LYTE WITH FLAVOR PACKS

    Dosage Form : FOR SOLUTION;ORAL

    Dosage Strength : 420GM/BOT;1.48GM/BOT;5.72GM/BOT;11.2GM/BOT

    Packaging :

    Approval Date : 2010-02-25

    Application Number : 79232

    Regulatory Info : DISCN

    Registration Country : USA

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    19

    Salix Pharmaceuticals

    U.S.A
    The Generic Rx Session
    Not Confirmed
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    Salix Pharmaceuticals

    U.S.A
    arrow
    The Generic Rx Session
    Not Confirmed
    • fda
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    Regulatory Info : RX

    Registration Country : USA

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

    Brand Name : MOVIPREP

    Dosage Form : FOR SOLUTION;ORAL

    Dosage Strength : 4.7GM;100GM;1.015GM;5.9GM;2.691GM;7.5GM

    Packaging :

    Approval Date : 2006-08-02

    Application Number : 21881

    Regulatory Info : RX

    Registration Country : USA

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    20

    Sandoz B2B

    Switzerland
    The Generic Rx Session
    Not Confirmed
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    Sandoz B2B

    Switzerland
    arrow
    The Generic Rx Session
    Not Confirmed
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    Regulatory Info : DISCN

    Registration Country : USA

    POLYETHYLENE GLYCOL 3350; POTASSIUM CHLORIDE; SODIUM BICARBONATE; SODIUM CHLORIDE; SODIUM SULFATE ANHYDROUS

    Brand Name : PEG-LYTE

    Dosage Form : FOR SUSPENSION;ORAL

    Dosage Strength : 236GM/BOT;2.97GM/BOT;6.74GM/BOT;5.86GM/BOT;22.74GM/BOT

    Packaging :

    Approval Date : 1993-08-31

    Application Number : 73098

    Regulatory Info : DISCN

    Registration Country : USA

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    21

    Vintage Pharmaceuticals-Charlotte

    U.S.A
    The Generic Rx Session
    Not Confirmed
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    Vintage Pharmaceuticals-Charlotte

    U.S.A
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    The Generic Rx Session
    Not Confirmed
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    Regulatory Info : DISCN

    Registration Country : USA

    POLYETHYLENE GLYCOL 3350; POTASSIUM CHLORIDE; SODIUM BICARBONATE; SODIUM CHLORIDE; SODIUM SULFATE ANHYDROUS

    Brand Name : CO-LAV

    Dosage Form : FOR SUSPENSION;ORAL

    Dosage Strength : 240GM/BOT;2.98GM/BOT;6.72GM/BOT;5.84GM/BOT;22.72GM/BOT

    Packaging :

    Approval Date : 1992-01-28

    Application Number : 73428

    Regulatory Info : DISCN

    Registration Country : USA

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    22

    Vintage Pharmaceuticals-Charlotte

    U.S.A
    The Generic Rx Session
    Not Confirmed
    arrow

    Vintage Pharmaceuticals-Charlotte

    U.S.A
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    The Generic Rx Session
    Not Confirmed
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    Regulatory Info : DISCN

    Registration Country : USA

    POLYETHYLENE GLYCOL 3350; POTASSIUM CHLORIDE; SODIUM BICARBONATE; SODIUM CHLORIDE; SODIUM SULFATE ANHYDROUS

    Brand Name : GO-EVAC

    Dosage Form : FOR SUSPENSION;ORAL

    Dosage Strength : 236GM/BOT;2.97GM/BOT;6.74GM/BOT;5.86GM/BOT;22.74GM/BOT

    Packaging :

    Approval Date : 1992-04-28

    Application Number : 73433

    Regulatory Info : DISCN

    Registration Country : USA

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    23

    NORVIUM BIOSCIENCE

    Country
    The Generic Rx Session
    Not Confirmed
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    NORVIUM BIOSCIENCE

    Country
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    The Generic Rx Session
    Not Confirmed
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    Regulatory Info : DISCN

    Registration Country : USA

    POLYETHYLENE GLYCOL 3350; POTASSIUM CHLORIDE; SODIUM BICARBONATE; SODIUM CHLORIDE; SODIUM SULFATE ANHYDROUS

    Brand Name : COLYTE

    Dosage Form : FOR SOLUTION;ORAL

    Dosage Strength : 227.1GM/PACKET;2.82GM/PACKET;6.36GM/PACKET;5.53GM/PACKET;21.5GM/PACKET **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons**

    Packaging :

    Approval Date : 1984-10-26

    Application Number : 18983

    Regulatory Info : DISCN

    Registration Country : USA

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    24

    NORVIUM BIOSCIENCE

    Country
    The Generic Rx Session
    Not Confirmed
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    NORVIUM BIOSCIENCE

    Country
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    The Generic Rx Session
    Not Confirmed
    • fda
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    Regulatory Info : DISCN

    Registration Country : USA

    POLYETHYLENE GLYCOL 3350; POTASSIUM CHLORIDE; SODIUM BICARBONATE; SODIUM CHLORIDE; SODIUM SULFATE ANHYDROUS

    Brand Name : COLYTE

    Dosage Form : FOR SOLUTION;ORAL

    Dosage Strength : 120GM/PACKET;1.49GM/PACKET;3.36GM/PACKET;2.92GM/PACKET;11.36GM/PACKET **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons**

    Packaging :

    Approval Date : 1984-10-26

    Application Number : 18983

    Regulatory Info : DISCN

    Registration Country : USA

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    25

    NORVIUM BIOSCIENCE

    Country
    The Generic Rx Session
    Not Confirmed
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    NORVIUM BIOSCIENCE

    Country
    arrow
    The Generic Rx Session
    Not Confirmed
    • fda
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    Regulatory Info : DISCN

    Registration Country : USA

    POLYETHYLENE GLYCOL 3350; POTASSIUM CHLORIDE; SODIUM BICARBONATE; SODIUM CHLORIDE; SODIUM SULFATE ANHYDROUS

    Brand Name : COLYTE

    Dosage Form : FOR SOLUTION;ORAL

    Dosage Strength : 360GM/PACKET;4.47GM/PACKET;10.08GM/PACKET;8.76GM/PACKET;34.08GM/PACKET **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons**

    Packaging :

    Approval Date : 1984-10-26

    Application Number : 18983

    Regulatory Info : DISCN

    Registration Country : USA

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    26

    NORVIUM BIOSCIENCE

    Country
    The Generic Rx Session
    Not Confirmed
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    NORVIUM BIOSCIENCE

    Country
    arrow
    The Generic Rx Session
    Not Confirmed
    • fda
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    Regulatory Info : DISCN

    Registration Country : USA

    POLYETHYLENE GLYCOL 3350; POTASSIUM CHLORIDE; SODIUM BICARBONATE; SODIUM CHLORIDE; SODIUM SULFATE ANHYDROUS

    Brand Name : COLYTE

    Dosage Form : FOR SOLUTION;ORAL

    Dosage Strength : 240GM/BOT;2.98GM/BOT;6.72GM/BOT;5.84GM/BOT;22.72GM/BOT **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons**

    Packaging :

    Approval Date : 1987-06-12

    Application Number : 18983

    Regulatory Info : DISCN

    Registration Country : USA

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    27

    NORVIUM BIOSCIENCE

    Country
    The Generic Rx Session
    Not Confirmed
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    NORVIUM BIOSCIENCE

    Country
    arrow
    The Generic Rx Session
    Not Confirmed
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    Regulatory Info : DISCN

    Registration Country : USA

    POLYETHYLENE GLYCOL 3350; POTASSIUM CHLORIDE; SODIUM BICARBONATE; SODIUM CHLORIDE; SODIUM SULFATE ANHYDROUS

    Brand Name : COLYTE-FLAVORED

    Dosage Form : FOR SOLUTION;ORAL

    Dosage Strength : 227.1GM/BOT;2.82GM/BOT;6.36GM/BOT;5.53GM/BOT;21.5GM/BOT **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons**

    Packaging :

    Approval Date : 1991-11-14

    Application Number : 18983

    Regulatory Info : DISCN

    Registration Country : USA

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    28

    NORVIUM BIOSCIENCE

    Country
    The Generic Rx Session
    Not Confirmed
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    NORVIUM BIOSCIENCE

    Country
    arrow
    The Generic Rx Session
    Not Confirmed
    • fda
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    Regulatory Info : DISCN

    Registration Country : USA

    POLYETHYLENE GLYCOL 3350; POTASSIUM CHLORIDE; SODIUM BICARBONATE; SODIUM CHLORIDE; SODIUM SULFATE ANHYDROUS

    Brand Name : COLYTE-FLAVORED

    Dosage Form : FOR SOLUTION;ORAL

    Dosage Strength : 240GM/BOT;2.98GM/BOT;6.72GM/BOT;5.84GM/BOT;22.72GM/BOT **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons**

    Packaging :

    Approval Date : 1991-11-14

    Application Number : 18983

    Regulatory Info : DISCN

    Registration Country : USA

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    29

    NORVIUM BIOSCIENCE

    Country
    The Generic Rx Session
    Not Confirmed
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    NORVIUM BIOSCIENCE

    Country
    arrow
    The Generic Rx Session
    Not Confirmed
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    Regulatory Info : DISCN

    Registration Country : USA

    POLYETHYLENE GLYCOL 3350; POTASSIUM CHLORIDE; SODIUM BICARBONATE; SODIUM CHLORIDE; SODIUM SULFATE ANHYDROUS

    Brand Name : COLYTE

    Dosage Form : FOR SOLUTION;ORAL

    Dosage Strength : 227.1GM/BOT;2.82GM/BOT;6.36GM/BOT;5.53GM/BOT;21.5GM/BOT **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons**

    Packaging :

    Approval Date : 1989-01-31

    Application Number : 18983

    Regulatory Info : DISCN

    Registration Country : USA

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    30

    NORVIUM BIOSCIENCE

    Country
    The Generic Rx Session
    Not Confirmed
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    NORVIUM BIOSCIENCE

    Country
    arrow
    The Generic Rx Session
    Not Confirmed
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    Regulatory Info : DISCN

    Registration Country : USA

    POLYETHYLENE GLYCOL 3350; POTASSIUM CHLORIDE; SODIUM BICARBONATE; SODIUM CHLORIDE; SODIUM SULFATE ANHYDROUS

    Brand Name : COLYTE WITH FLAVOR PACKS

    Dosage Form : FOR SOLUTION;ORAL

    Dosage Strength : 240GM/BOT;2.98GM/BOT;6.72GM/BOT;5.84GM/BOT;22.72GM/BOT

    Packaging :

    Approval Date : 1998-10-08

    Application Number : 18983

    Regulatory Info : DISCN

    Registration Country : USA

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