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01 3APOTEX INC

02 3GLENWOOD GMBH PHARMAZEUTISCHE ERZEUGNISSE

03 2SANDOZ CANADA INCORPORATED

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PharmaCompass

01

Interphex
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FELODIPINE

Brand Name : APO-FELODIPINE

Dosage Form : TABLET (EXTENDED-RELEASE)

Dosage Strength : 10MG

Packaging : 100

Approval Date :

Application Number : 2452383

Regulatory Info : Prescription

Registration Country : Canada

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02

Interphex
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Interphex
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FELODIPINE

Brand Name : APO-FELODIPINE

Dosage Form : TABLET (EXTENDED-RELEASE)

Dosage Strength : 2.5MG

Packaging : 100

Approval Date :

Application Number : 2452367

Regulatory Info : Prescription

Registration Country : Canada

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03

Interphex
Not Confirmed
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Interphex
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FELODIPINE

Brand Name : APO-FELODIPINE

Dosage Form : TABLET (EXTENDED-RELEASE)

Dosage Strength : 5MG

Packaging : 100

Approval Date :

Application Number : 2452375

Regulatory Info : Prescription

Registration Country : Canada

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04

Interphex
Not Confirmed
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Interphex
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FELODIPINE

Brand Name : PLENDIL

Dosage Form : TABLET (EXTENDED-RELEASE)

Dosage Strength : 2.5MG

Packaging :

Approval Date :

Application Number : 2057778

Regulatory Info : Prescription

Registration Country : Canada

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05

Interphex
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Interphex
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FELODIPINE

Brand Name : PLENDIL

Dosage Form : TABLET (EXTENDED-RELEASE)

Dosage Strength : 5MG

Packaging :

Approval Date :

Application Number : 851779

Regulatory Info : Prescription

Registration Country : Canada

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06

Interphex
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Interphex
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FELODIPINE

Brand Name : PLENDIL

Dosage Form : TABLET (EXTENDED-RELEASE)

Dosage Strength : 10MG

Packaging :

Approval Date :

Application Number : 851787

Regulatory Info : Prescription

Registration Country : Canada

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07

Interphex
Not Confirmed
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Interphex
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FELODIPINE

Brand Name : SANDOZ FELODIPINE

Dosage Form : TABLET (EXTENDED-RELEASE)

Dosage Strength : 5MG

Packaging : 30/100

Approval Date :

Application Number : 2280264

Regulatory Info : Prescription

Registration Country : Canada

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08

Interphex
Not Confirmed
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Interphex
Not Confirmed

FELODIPINE

Brand Name : SANDOZ FELODIPINE

Dosage Form : TABLET (EXTENDED-RELEASE)

Dosage Strength : 10MG

Packaging : 30/100

Approval Date :

Application Number : 2280272

Regulatory Info : Prescription

Registration Country : Canada

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