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01 2Strides Pharma Science

02 1TAPI Technology & API Services

03 1ANGITA PHARMA INC.

04 1Aralez Pharmaceuticals

05 1Aurobindo Pharma Limited

06 7BRAINTREE LABS

07 1Bayer AG

08 1CellChem Pharmaceuticals

09 1Dynapharm

10 1E-Z-EM Canada Inc, dba Therapex

11 2Extrovis AG

12 1Hanlim Pharmaceuticals Inc

13 1Hospira, Inc.

14 1JAMP PHARMA

15 2Johnson & Johnson

16 2Juno Pharmaceuticals Pty Ltd

17 1MANTRA PHARMA INC

18 1MEDEXUS PHARMACEUTICALS INC.

19 1Medisca

20 1Norgine

21 8Norvium

22 6Novel Laboratories, Inc.

23 3PENDOPHARM DIVISION OF DE PHARMASCIENCE INC

24 4Perrigo Company plc

25 1Pharmascience Inc.

26 1SOLIS PHARMS

27 2Salix Pharmaceuticals

28 1Sandoz B2B

29 1Taro Pharmaceutical Industries

30 2Vintage Pharmaceuticals-Charlotte

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PharmaCompass

01

  • fda
  • EDQM
  • WHO-GMP

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

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

02

  • 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

03

  • fda
  • EDQM
  • WHO-GMP

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

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 : 2015-04-13

Application Number : 204559

Regulatory Info : RX

Registration Country : USA

Strides Pharma Science

04

Discovery Europe
Not Confirmed
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Discovery Europe
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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05

Discovery Europe
Not Confirmed
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Discovery Europe
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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06

Discovery Europe
Not Confirmed
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Discovery Europe
Not Confirmed

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

Packaging :

Approval Date : 1991-04-22

Application Number : 19797

Regulatory Info : RX

Registration Country : USA

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07

Discovery Europe
Not Confirmed
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Discovery Europe
Not Confirmed

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

Packaging :

Approval Date : 1994-11-18

Application Number : 19797

Regulatory Info : RX

Registration Country : USA

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08

Discovery Europe
Not Confirmed
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Discovery Europe
Not Confirmed

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

Packaging :

Approval Date :

Application Number : 21551

Regulatory Info :

Registration Country : USA

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09

Discovery Europe
Not Confirmed
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Discovery Europe
Not Confirmed

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**

Packaging :

Approval Date : 2010-07-16

Application Number : 21551

Regulatory Info : DISCN

Registration Country : USA

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10

Discovery Europe
Not Confirmed
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Discovery Europe
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

Discovery Europe
Not Confirmed
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Discovery Europe
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

Discovery Europe
Not Confirmed
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Discovery Europe
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

Discovery Europe
Not Confirmed
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Discovery Europe
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

Discovery Europe
Not Confirmed
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Discovery Europe
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

Discovery Europe
Not Confirmed
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Discovery Europe
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

Discovery Europe
Not Confirmed
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Discovery Europe
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

Discovery Europe
Not Confirmed
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Discovery Europe
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

Discovery Europe
Not Confirmed
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Discovery Europe
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

Discovery Europe
Not Confirmed
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Discovery Europe
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

Discovery Europe
Not Confirmed
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Discovery Europe
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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