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01 1STRIDES PHARMA

02 1ALKEM LABS LTD

03 1ANNORA PHARMA

04 1BIONPHARMA

05 2BRAINTREE LABS

06 1GATOR PHARMS

07 1NOVEL LABS INC

08 1PADDOCK LLC

09 1PAI HOLDINGS

10 1TARO

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PharmaCompass

01

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PharmaVenue
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

02

PharmaVenue
Not Confirmed
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PharmaVenue
Not Confirmed

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 : 2024-10-18

Application Number : 212903

RX/OTC/DISCN : RX

RLD : No

TE Code : AA

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03

PharmaVenue
Not Confirmed
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PharmaVenue
Not Confirmed

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 : 2024-06-24

Application Number : 204135

RX/OTC/DISCN : RX

RLD : No

TE Code : AA

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04

PharmaVenue
Not Confirmed
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PharmaVenue
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

Approval Date : 2010-08-05

Application Number : 22372

RX/OTC/DISCN : RX

RLD : Yes

TE Code : AA

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05

PharmaVenue
Not Confirmed
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PharmaVenue
Not Confirmed

MAGNESIUM SULFATE; POLYETHYLENE GLYCOL 3350; POTASSIUM CHLORIDE; POTASSIUM SULFATE; SODIUM BICARBONATE; SODIUM CHLORIDE; SODIUM SULFATE

Brand Name : SUCLEAR

Dosage Form : SOLUTION;ORAL

Dosage Strength : 1.6GM/BOT,3.13GM/BOT,17.5GM/BOT,N/A,N/A,N/A,N/A;N/A,N/A,N/A,210GM,0.74GM,2.86GM,5.6GM **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reason

Approval Date : 2013-01-18

Application Number : 203595

RX/OTC/DISCN : DISCN

RLD : Yes

TE Code :

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06

PharmaVenue
Not Confirmed
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PharmaVenue
Not Confirmed

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 : 2017-02-23

Application Number : 202511

RX/OTC/DISCN : RX

RLD : No

TE Code : AA

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07

PharmaVenue
Not Confirmed
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PharmaVenue
Not Confirmed

MAGNESIUM SULFATE ANHYDROUS; POTASSIUM SULFATE; SODIUM SULFATE

Brand Name : MAGNESIUM SULFATE ANHYDROUS; POTASSIUM SULFATE; SODIUM SULFATE

Dosage Form : SOLUTION;ORAL

Dosage Strength : 1.6GM/BOT; 3.13GM/BOT; 17.5GM/BOT

Approval Date :

Application Number : 203102

RX/OTC/DISCN :

RLD :

TE Code :

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08

PharmaVenue
Not Confirmed
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PharmaVenue
Not Confirmed

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 : 2024-03-19

Application Number : 206431

RX/OTC/DISCN : RX

RLD : No

TE Code : AA

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09

GATOR PHARMS

Country
PharmaVenue
Not Confirmed
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GATOR PHARMS

Country
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PharmaVenue
Not Confirmed

MAGNESIUM SULFATE; POTASSIUM SULFATE; SODIUM SULFATE

Brand Name : COLPREP KIT

Dosage Form : POWDER;ORAL

Dosage Strength : 1.6GM/BOT;3.13GM/BOT;17.5GM/BOT

Approval Date : 2016-12-27

Application Number : 204553

RX/OTC/DISCN : DISCN

RLD : Yes

TE Code :

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10

PAI HOLDINGS

Country
PharmaVenue
Not Confirmed
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PAI HOLDINGS

Country
arrow
PharmaVenue
Not Confirmed

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 : 2024-07-15

Application Number : 209941

RX/OTC/DISCN : RX

RLD : No

TE Code : AA

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