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01 2Aspen Pharmacare Holdings

02 1Shandong Loncom Pharmaceutical

03 3Strides Pharma Science

04 1TAPI Technology & API Services

05 12care4

06 1ABC Farmaceutici SpA

07 1Abacus Medicine

08 2Alfasigma

09 1Alkem Laboratories

10 1Annora Pharma

11 1Aralez Pharmaceuticals

12 4Azurity Pharma

13 1BRAINTREE LABS

14 1Bionpharma

15 1Bohm Laboratories Sa

16 2Cps Cito Pharma Services Gmbh

17 1Dynapharm

18 1E-Z-EM Canada Inc, dba Therapex

19 1EJ Busuttil Ltd

20 1Extrovis AG

21 1GATOR PHARMS

22 2Giuliani

23 1Hospira, Inc.

24 2Ipsen

25 2JAMP PHARMA

26 4Karo Pharma

27 2Laboratorios ERN

28 1Mayoly Spindler

29 1Medicem

30 19Norgine

31 4Novel Laboratories, Inc.

32 1ORIFARM GROUP AS

33 1P & D Pharmaceuticals Limited

34 1PAI HOLDINGS

35 3PROMEFARM Srl

36 3Pendopharm

37 3Perrigo Company plc

38 1Pharmacodynamic Applications Laboratory Sa

39 8Quagen Pharma

40 1Recordati

41 2Salix Pharmaceuticals

42 1Sandoz B2B

43 1Spirig Healthcare

44 2Taro Pharmaceutical Industries

45 2Vintage Pharmaceuticals-Charlotte

46 1World Medicine

47 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 BoothShandong Loncom is an R&D-focused manufacturer of Anti-cancer APIs.

Regulatory Info :

Registration Country : China

Magnesium Sulfate; Sodium Sulfate; Potassium Sulfate

Brand Name : Magnesium Sulfate; Sodium Sulfate; Potassium Sulfate

Dosage Form : Oral Solution

Dosage Strength : 3.276G/176ML; 17.51G/176ML; 3.13G/176ML

Packaging :

Approval Date :

Application Number :

Regulatory Info :

Registration Country : China

Shandong Loncom Pharmaceutical company banner

03

  • 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

04

  • 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

05

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

06

  • 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

07

  • 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

08

RDD
Not Confirmed
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RDD
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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09

RDD
Not Confirmed
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RDD
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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10

RDD
Not Confirmed
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RDD
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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11

RDD
Not Confirmed
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RDD
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

RDD
Not Confirmed
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RDD
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

RDD
Not Confirmed
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RDD
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

RDD
Not Confirmed
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RDD
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

RDD
Not Confirmed
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RDD
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

RDD
Not Confirmed
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RDD
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

RDD
Not Confirmed
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RDD
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

RDD
Not Confirmed
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RDD
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

RDD
Not Confirmed
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RDD
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

RDD
Not Confirmed
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RDD
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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