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01 2STRIDES PHARMA

02 1GOLDLINE

03 1ALKEM LABS LTD

04 1ANNORA PHARMA

05 1BIONPHARMA

06 2BRAINTREE

07 3BRAINTREE LABS

08 1DYNAPHARM

09 1E Z EM

10 1GATOR PHARMS

11 1HOSPIRA

12 8NORVIUM BIOSCIENCE

13 4NOVEL LABS INC

14 3PADDOCK LLC

15 1PAI HOLDINGS

16 1RISING

17 1SALIX

18 1SALIX PHARMS

19 1SANDOZ

20 2TARO

21 2VINTAGE PHARMS

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PharmaCompass

01

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Antibody Engineering
Not Confirmed
  • fda
  • EDQM
  • WHO-GMP

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

RLD : No

TE Code : AA

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

Approval Date : 2018-12-21

Application Number : 204558

RX/OTC/DISCN : RX

RLD : No

TE Code : AA

Strides Pharma Science

02

  • fda
  • EDQM
  • WHO-GMP

Virtual BoothTAPI offers customized CDMO Solutions for API development and manufacturing services.

RLD : No

TE Code :

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

Approval Date : 1988-12-23

Application Number : 72319

RX/OTC/DISCN : DISCN

RLD : No

TE Code :

TAPI Company Banner

03

arrow
Antibody Engineering
Not Confirmed
  • fda
  • EDQM
  • WHO-GMP

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

RLD : No

TE Code : AA

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

Approval Date : 2023-11-22

Application Number : 215469

RX/OTC/DISCN : RX

RLD : No

TE Code : AA

Strides Pharma Science

04

NORVIUM BIOSCIENCE

Country
Antibody Engineering
Not Confirmed
arrow

NORVIUM BIOSCIENCE

Country
arrow
Antibody Engineering
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**

Approval Date : 1984-10-26

Application Number : 18983

RX/OTC/DISCN : DISCN

RLD : No

TE Code :

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05

NORVIUM BIOSCIENCE

Country
Antibody Engineering
Not Confirmed
arrow

NORVIUM BIOSCIENCE

Country
arrow
Antibody Engineering
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**

Approval Date : 1984-10-26

Application Number : 18983

RX/OTC/DISCN : DISCN

RLD : No

TE Code :

blank

06

NORVIUM BIOSCIENCE

Country
Antibody Engineering
Not Confirmed
arrow

NORVIUM BIOSCIENCE

Country
arrow
Antibody Engineering
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**

Approval Date : 1984-10-26

Application Number : 18983

RX/OTC/DISCN : DISCN

RLD : No

TE Code :

blank

07

NORVIUM BIOSCIENCE

Country
Antibody Engineering
Not Confirmed
arrow

NORVIUM BIOSCIENCE

Country
arrow
Antibody Engineering
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**

Approval Date : 1987-06-12

Application Number : 18983

RX/OTC/DISCN : DISCN

RLD : No

TE Code :

blank

08

NORVIUM BIOSCIENCE

Country
Antibody Engineering
Not Confirmed
arrow

NORVIUM BIOSCIENCE

Country
arrow
Antibody Engineering
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**

Approval Date : 1991-11-14

Application Number : 18983

RX/OTC/DISCN : DISCN

RLD : No

TE Code :

blank

09

NORVIUM BIOSCIENCE

Country
Antibody Engineering
Not Confirmed
arrow

NORVIUM BIOSCIENCE

Country
arrow
Antibody Engineering
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**

Approval Date : 1991-11-14

Application Number : 18983

RX/OTC/DISCN : DISCN

RLD : No

TE Code :

blank

10

NORVIUM BIOSCIENCE

Country
Antibody Engineering
Not Confirmed
arrow

NORVIUM BIOSCIENCE

Country
arrow
Antibody Engineering
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**

Approval Date : 1989-01-31

Application Number : 18983

RX/OTC/DISCN : DISCN

RLD : No

TE Code :

blank