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01 2Aspen Pharmacare Holdings
02 2Strides Pharma Science
03 1TAPI Technology & API Services
04 1ABC Farmaceutici SpA
05 2Alfasigma
06 1Alkem Laboratories
07 1Annora Pharma
08 1Aralez Pharmaceuticals
09 5BRAINTREE LABS
10 1Bionpharma
11 1Bohm Laboratories Sa
12 2Cps Cito Pharma Services Gmbh
13 1Dynapharm
14 1E-Z-EM Canada Inc, dba Therapex
15 1Extrovis AG
16 1GATOR PHARMS
17 2Giuliani
18 1Hospira, Inc.
19 1Ipsen
20 2JAMP PHARMA
21 1Karo Pharma
22 2Laboratorios ERN
23 12Norgine
24 8Norvium
25 4Novel Laboratories, Inc.
26 1PAI HOLDINGS
27 3PROMEFARM Srl
28 3Pendopharm
29 3Perrigo Company plc
30 1Recordati
31 2Salix Pharmaceuticals
32 1Sandoz B2B
33 1Spirig Healthcare
34 2Taro Pharmaceutical Industries
35 2Vintage Pharmaceuticals-Charlotte
36 1World Medicine
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01 2Effervescent Granule
02 20FOR SOLUTION;ORAL
03 6FOR SUSPENSION;ORAL
04 1INJECTABLE
05 1KIT
06 1Oral Powder
07 8Oral Solution
08 1POW
09 1POWDER
10 4POWDER FOR SOLUTION
11 1POWDER;ORAL
12 3Powder
13 8Powder For Oral Solution
14 1SAC
15 11SOLUTION;ORAL
16 1TABLET;ORAL
17 7Blank
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01 7Allowed
02 4Approved
03 8Authorized
04 1Cancelled
05 22DISCN
06 1Deregistered
07 6Ethical
08 1Generic
09 2Originator
10 16RX
11 1Suspensed
12 8Blank
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01 1BI-PEGLYTE
02 1Bohm Evacuating Solution Powder For Oral Solution In Sachets
03 1CLENZ-LYTE
04 1CO-LAV
05 1COLOVAGE
06 1COLPREP KIT
07 6COLYTE
08 1COLYTE WITH FLAVOR PACKS
09 2COLYTE-FLAVORED
10 1Casenglycol Powder For Oral Solution
11 1Clensia
12 1Clensia Powder For Oral Solution
13 1Cololyt
14 1Concentrated Eziclen For Oral Solution
15 1E-Z-EM PREP LYTE
16 1GLYCOPREP
17 1GO-EVAC
18 2GOLYTELY
19 2Isocolan
20 1JAMPLYTE
21 1JAMPLYTE + BISACODYL
22 1Klean Prep
23 1Klean-prep
24 1Laxative
25 1Lebersal Effervescent Granulated Lemon Flavor
26 1Lebersal Effervescent Granules Orange Flavor
27 1MAGNESIUM SULFATE ANHYDROUS; POTASSIUM SULFATE; SODIUM SULFATE
28 3MOVIPREP
29 2Moviprep
30 1Moviprep Orange
31 1Moviprep Orange Flavor Powder For Oral Solution
32 2Moviprep Powder For Oral Solution
33 1Movprep
34 1Movprep Orange
35 1OCL
36 3PEG 3350 AND ELECTROLYTES
37 2PEG-3350, SODIUM SULFATE, SODIUM CHLORIDE, POTASSIUM CHLORIDE, SODIUM ASCORBATE AND ASCORBIC ACID
38 1PEG-LYTE
39 1PEGLYTE POWDER
40 1PLENVU
41 2POLYETHYLENE GLYCOL 3350 AND ELECTROLYTES
42 1Pleinvue Powder For Oral Solution
43 2Plenvu
44 1Polyethylene Glycol + Salts Sodium/Potassium
45 7SODIUM SULFATE, POTASSIUM SULFATE AND MAGNESIUM SULFATE
46 1SUCLEAR
47 1SUPREP BOWEL PREP KIT
48 1SUTAB
49 2Selg
50 1Selg They
51 1Transipeg
52 1Transipeg forte
53 1Blank
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01 6Canada
02 7Italy
03 2South Africa
04 10Spain
05 5Sweden
06 7Switzerland
07 1Turkey
08 39USA
Regulatory Info : Originator
Registration Country : South Africa
Brand Name : MOVIPREP
Dosage Form : POW
Dosage Strength : 7.5g
Packaging : 1X1g
Approval Date :
Application Number :
Regulatory Info : Originator
Registration Country : South Africa
Regulatory Info : RX
Registration Country : USA
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
Packaging :
Approval Date : 2018-12-21
Application Number : 204558
Regulatory Info : RX
Registration Country : USA
TAPI, a leading global supplier of APIs, provides over 350 products and customized CDMO solutions for every stage of development.
Regulatory Info : DISCN
Registration Country : USA
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
Packaging :
Approval Date : 1988-12-23
Application Number : 72319
Regulatory Info : DISCN
Registration Country : USA
Regulatory Info : Originator
Registration Country : South Africa
Brand Name : Klean-prep
Dosage Form : SAC
Dosage Strength : 5.685g
Packaging : 4X1g
Approval Date :
Application Number :
Regulatory Info : Originator
Registration Country : South Africa
Regulatory Info : RX
Registration Country : USA
MAGNESIUM SULFATE; POTASSIUM SULFATE; SODIUM SULFATE
Brand Name : SODIUM SULFATE, POTASSIUM SULFATE AND MAGNESIUM SULFATE
Dosage Form : SOLUTION;ORAL
Dosage Strength : 1.6GM/BOT;3.13GM/BOT;17.5GM/BOT
Packaging :
Approval Date : 2023-11-22
Application Number : 215469
Regulatory Info : RX
Registration Country : USA
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
Packaging :
Approval Date : 1984-07-13
Application Number : 19011
Regulatory Info : RX
Registration Country : USA
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
Packaging :
Approval Date : 1992-06-02
Application Number : 19011
Regulatory Info : DISCN
Registration Country : USA
Regulatory Info : RX
Registration Country : USA
MAGNESIUM SULFATE; POTASSIUM SULFATE; SODIUM SULFATE
Brand Name : SUPREP BOWEL PREP KIT
Dosage Form : SOLUTION;ORAL
Dosage Strength : 1.6GM/BOT;3.13GM/BOT;17.5GM/BOT
Packaging :
Approval Date : 2010-08-05
Application Number : 22372
Regulatory Info : RX
Registration Country : USA
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
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
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
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
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
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
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
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
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
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
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
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