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01 5AFT Pharmaceuticals

02 1E.C. De Witt & Co. Ltd.

03 1Johnson & Johnson

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PharmaCompass

01

BOS Manchester
Not Confirmed
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BOS Manchester
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citric acid + lauryl sulfoacetate sodium + sorbitol

Brand Name : Micolette

Dosage Form : Enema

Dosage Strength : 90MG/1ML

Packaging : 1

Approval Date :

Application Number :

Regulatory Info :

Registration Country : Australia

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02

BOS Manchester
Not Confirmed
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BOS Manchester
Not Confirmed

citric acid + lauryl sulfoacetate sodium + sorbitol

Brand Name : Micolette

Dosage Form : Enema

Dosage Strength : 90MG/1ML

Packaging : 1

Approval Date :

Application Number :

Regulatory Info :

Registration Country : Australia

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03

BOS Manchester
Not Confirmed
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BOS Manchester
Not Confirmed

citric acid + lauryl sulfoacetate sodium + sorbitol

Brand Name : Micolette

Dosage Form : Enema

Dosage Strength : 90MG/1ML

Packaging : 1

Approval Date :

Application Number :

Regulatory Info :

Registration Country : Australia

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04

BOS Manchester
Not Confirmed
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BOS Manchester
Not Confirmed

citric acid + lauryl sulfoacetate sodium + sorbitol

Brand Name : Micolette

Dosage Form :

Dosage Strength :

Packaging : 1

Approval Date :

Application Number :

Regulatory Info :

Registration Country : Australia

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05

BOS Manchester
Not Confirmed
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BOS Manchester
Not Confirmed

citric acid + lauryl sulfoacetate sodium + sorbitol

Brand Name : Micolette

Dosage Form : Enema

Dosage Strength : 90MG/1ML

Packaging : 1

Approval Date :

Application Number :

Regulatory Info :

Registration Country : Australia

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06

BOS Manchester
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BOS Manchester
Not Confirmed

Sodium Citrate Dihydrate; Sodium Lauryl Sulfoacetate

Brand Name : Microlax

Dosage Form : Rectal Solution

Dosage Strength :

Packaging :

Approval Date : 31/12/1963

Application Number : 19631231000026

Regulatory Info : Approved

Registration Country : Sweden

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07

E.C. De Witt & Co. Ltd.

Country
BOS Manchester
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E.C. De Witt & Co. Ltd.

Country
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BOS Manchester
Not Confirmed

Sodium Citrate Dihydrate; Sodium Lauryl Sulfoacetate

Brand Name : Fleet Micro

Dosage Form : Rectal Solution

Dosage Strength :

Packaging :

Approval Date : 28/02/1997

Application Number : 19970228000022

Regulatory Info : Deregistered

Registration Country : Sweden

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