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    Drug Approvals by the Medicines Control Council in South Africa containing Prednisolone. Original Data : South African Medicines Price Registry

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    Prednisolone

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    Pharmacare Limited, Woodmead

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    Regulatory Info : Generic

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    Prednisolone

    Brand Name : Lenisolone

    Dosage Form : TAB

    Dosage Strength : 5mg

    Packaging : 1000X1mg

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    Regulatory Info : Generic

    Registration Country : South Africa

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    Strides Pharma SA (Pty) Ltd

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    Prednisolone

    Brand Name : Prednisilone 15 Strides

    Dosage Form : SYR

    Dosage Strength : 15mg/5ml

    Packaging : 50X1mg/5ml

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    Prednisolone

    Brand Name : Prelone

    Dosage Form : TAB

    Dosage Strength : 5mg

    Packaging : 200X1mg

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    Registration Country : South Africa

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    Prednisolone

    Brand Name : Adco Prednisolone Syrup

    Dosage Form : SYR

    Dosage Strength : 15mg/5ml

    Packaging : 50X1mg/5ml

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    Prednisolone

    Brand Name : Prelone Syrup

    Dosage Form : SYR

    Dosage Strength : 15mg/5ml

    Packaging : 50X1mg/5ml

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    Regulatory Info : Generic

    Registration Country : South Africa

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    Prednisolone

    Brand Name : Prelone Syrup

    Dosage Form : SYR

    Dosage Strength : 15mg/5ml

    Packaging : 100X1mg/5ml

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    Regulatory Info : Generic

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    Regulatory Info : Originator

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    Prednisolone Caproate

    Brand Name : Scheriproct Oinment

    Dosage Form : OIN

    Dosage Strength : 1.9mg/g

    Packaging : 15X1mg/g

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    Regulatory Info : Originator

    Registration Country : South Africa

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    Regulatory Info : Originator

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    Prednisolone Caproate

    Brand Name : Scheriproct Ointment

    Dosage Form : OIN

    Dosage Strength : 1.9mg/g

    Packaging : 30X1mg/g

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    Regulatory Info : Originator

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    Prednisolone Caproate

    Brand Name : Scheriproct Suppositories

    Dosage Form : SUP

    Dosage Strength : 1.3mg

    Packaging : 12X1mg

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    Regulatory Info : Originator

    Registration Country : South Africa

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    Prednisolone Caproate

    Brand Name : Scheriproct Suppositories

    Dosage Form : SUP

    Dosage Strength : 1.3mg

    Packaging : 12X1mg

    Approval Date :

    Application Number :

    Regulatory Info : Originator

    Registration Country : South Africa

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