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01 2Aspen Pharmacare Holdings

02 3Strides 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 1EJ Busuttil Ltd

16 1Extrovis AG

17 1GATOR PHARMS

18 2Giuliani

19 1Hospira, Inc.

20 1Ipsen

21 2JAMP PHARMA

22 1Karo Pharma

23 2Laboratorios ERN

24 1Medicem

25 12Norgine

26 4Novel Laboratories, Inc.

27 1P & D Pharmaceuticals Limited

28 1PAI HOLDINGS

29 3PROMEFARM Srl

30 3Pendopharm

31 3Perrigo Company plc

32 8Quagen Pharma

33 1Recordati

34 2Salix Pharmaceuticals

35 1Sandoz B2B

36 1Spirig Healthcare

37 2Taro Pharmaceutical Industries

38 2Vintage Pharmaceuticals-Charlotte

39 1World Medicine

40 1Blank

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PharmaCompass

01

Sodium sulphate anhydrous

Brand Name : MOVIPREP

Dosage Form : POW

Dosage Strength : 7.5g

Packaging : 1X1g

Approval Date :

Application Number :

Regulatory Info : Originator

Registration Country : South Africa

Aspen API Comapny Banner

02

  • fda
  • EDQM
  • WHO-GMP

Virtual BoothSynergice, a Strides Pharma initiative, is a new gen B2B platform for diverse portofolio needs.

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

Strides Pharma Science

03

  • fda
  • EDQM
  • WHO-GMP

Virtual BoothTAPI, 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

TAPI Company Banner

04

Sodium Sulphate Anhydrous

Brand Name : Klean-prep

Dosage Form : SAC

Dosage Strength : 5.685g

Packaging : 4X1g

Approval Date :

Application Number :

Regulatory Info : Originator

Registration Country : South Africa

Aspen API Comapny Banner

05

  • fda
  • EDQM
  • WHO-GMP

Virtual BoothSynergice, a Strides Pharma initiative, is a new gen B2B platform for diverse portofolio needs.

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

Strides Pharma Science

06

  • fda
  • EDQM
  • WHO-GMP

Virtual BoothSynergice, a Strides Pharma initiative, is a new gen B2B platform for diverse portofolio needs.

Regulatory Info :

Registration Country : India

Sodium Sulfate; Potassium Sulfate; Magnesium Sulfate

Brand Name : Sodium Sulfate; Potassium Sulfate; Magnesium Sulfate

Dosage Form : Oral Solution

Dosage Strength : (17.5 g/3.13 g/1.6 g) per 6 ounces

Packaging :

Approval Date :

Application Number :

Regulatory Info :

Registration Country : India

Strides Pharma Science

07

Neuroscience
Not Confirmed
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Neuroscience
Not Confirmed

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

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08

Neuroscience
Not Confirmed
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Neuroscience
Not Confirmed

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

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09

Neuroscience
Not Confirmed
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Neuroscience
Not Confirmed

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

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10

Neuroscience
Not Confirmed
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Neuroscience
Not Confirmed

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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11

Neuroscience
Not Confirmed
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Neuroscience
Not Confirmed

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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12

Neuroscience
Not Confirmed
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Neuroscience
Not Confirmed

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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13

Neuroscience
Not Confirmed
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Neuroscience
Not Confirmed

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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14

Neuroscience
Not Confirmed
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Neuroscience
Not Confirmed

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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15

Neuroscience
Not Confirmed
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Neuroscience
Not Confirmed

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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16

Neuroscience
Not Confirmed
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Neuroscience
Not Confirmed

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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17

Neuroscience
Not Confirmed
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Neuroscience
Not Confirmed

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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18

Neuroscience
Not Confirmed
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Neuroscience
Not Confirmed

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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19

Neuroscience
Not Confirmed
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Neuroscience
Not Confirmed

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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20

Neuroscience
Not Confirmed
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Neuroscience
Not Confirmed

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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