Solifenacin Succinate

APOTEX INC

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CANADA

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Virtual Booth

Dosage Form

TABLET

Dosage Strength

5MG

Approval Date

Brand Name

APO-SOLIFENACIN

Application Number

2423375

Packaging Presentation

30/100

Regulatory Information

Prescription

Supporting Information

APOTEX INC

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CANADA

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SOLIFENACIN SUCCINATE

Dosage Form

TABLET

Dosage Strength

10MG

Approval Date

Brand Name

APO-SOLIFENACIN

Application Number

2423383

Packaging Presentation

30/100

Regulatory Information

Prescription

Supporting Information

ASTELLAS PHARMA CANADA INC

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JAPAN

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Virtual Booth

SOLIFENACIN SUCCINATE

Dosage Form

TABLET

Dosage Strength

5MG

Approval Date

Brand Name

VESICARE

Application Number

2277263

Packaging Presentation

30/90

Regulatory Information

Prescription

Supporting Information

ASTELLAS PHARMA CANADA INC

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JAPAN

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Virtual Booth

SOLIFENACIN SUCCINATE

Dosage Form

TABLET

Dosage Strength

10MG

Approval Date

Brand Name

VESICARE

Application Number

2277271

Packaging Presentation

30/90

Regulatory Information

Prescription

Supporting Information

AURO PHARMA INC

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INDIA

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Virtual Booth

SOLIFENACIN SUCCINATE

Dosage Form

TABLET

Dosage Strength

5MG

Approval Date

Brand Name

AURO-SOLIFENACIN

Application Number

2446375

Packaging Presentation

10/30/90/100/500/1000

Regulatory Information

Prescription

Supporting Information

AURO PHARMA INC

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INDIA

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Virtual Booth

SOLIFENACIN SUCCINATE

Dosage Form

TABLET

Dosage Strength

10MG

Approval Date

Brand Name

AURO-SOLIFENACIN

Application Number

2446383

Packaging Presentation

30/90/100/500/1000

Regulatory Information

Prescription

Supporting Information

JAMP PHARMA CORPORATION

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CANADA

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SOLIFENACIN SUCCINATE

Dosage Form

TABLET

Dosage Strength

5MG

Approval Date

Brand Name

JAMP-SOLIFENACIN

Application Number

2424339

Packaging Presentation

30/100/500

Regulatory Information

Prescription

Supporting Information

JAMP PHARMA CORPORATION

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CANADA

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SOLIFENACIN SUCCINATE

Dosage Form

TABLET

Dosage Strength

10MG

Approval Date

Brand Name

JAMP-SOLIFENACIN

Application Number

2424347

Packaging Presentation

30/100/500

Regulatory Information

Prescription

Supporting Information

MINT PHARMACEUTICALS INC

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CANADA

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SOLIFENACIN SUCCINATE

Dosage Form

TABLET

Dosage Strength

5MG

Approval Date

Brand Name

MINT-SOLIFENACIN

Application Number

2443171

Packaging Presentation

30/90

Regulatory Information

Prescription

Supporting Information

MINT PHARMACEUTICALS INC

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CANADA

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Virtual Booth

SOLIFENACIN SUCCINATE

Dosage Form

TABLET

Dosage Strength

10MG

Approval Date

Brand Name

MINT-SOLIFENACIN

Application Number

2443198

Packaging Presentation

30/90

Regulatory Information

Prescription

Supporting Information

Pharmascience Inc.

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CANADA

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Virtual Booth

Solifenacin

Dosage Form

TABLET

Dosage Strength

5MG

Approval Date

Brand Name

Application Number

Packaging Presentation

Regulatory Information

Generic

Supporting Information

View All

Canadian Dossier Based

Pharmascience Inc.

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CANADA

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Virtual Booth

Solifenacin

Dosage Form

TABLET

Dosage Strength

10MG

Approval Date

Brand Name

Application Number

Packaging Presentation

Regulatory Information

Generic

Supporting Information

View All

Canadian Dossier Based

PHARMASCIENCE INC

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CANADA

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Virtual Booth

SOLIFENACIN SUCCINATE

Dosage Form

TABLET

Dosage Strength

5MG

Approval Date

Brand Name

PMS-SOLIFENACIN

Application Number

2417723

Packaging Presentation

30/100

Regulatory Information

Prescription

Supporting Information

PHARMASCIENCE INC

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CANADA

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SOLIFENACIN SUCCINATE

Dosage Form

TABLET

Dosage Strength

10MG

Approval Date

Brand Name

PMS-SOLIFENACIN

Application Number

2417731

Packaging Presentation

30/100

Regulatory Information

Prescription

Supporting Information

PRO DOC LIMITEE

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CANADA

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Virtual Booth

SOLIFENACIN SUCCINATE

Dosage Form

TABLET

Dosage Strength

5MG

Approval Date

Brand Name

SOLIFENACIN

Application Number

2458144

Packaging Presentation

30/100

Regulatory Information

Prescription

Supporting Information

PRO DOC LIMITEE

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CANADA

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Virtual Booth

SOLIFENACIN SUCCINATE

Dosage Form

TABLET

Dosage Strength

10MG

Approval Date

Brand Name

SOLIFENACIN

Application Number

2458152

Packaging Presentation

30/100

Regulatory Information

Prescription

Supporting Information

RANBAXY PHARMACEUTICALS CANADA INC.

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INDIA

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Virtual Booth

SOLIFENACIN SUCCINATE

Dosage Form

TABLET

Dosage Strength

5MG

Approval Date

Brand Name

RAN-SOLIFENACIN

Application Number

2437988

Packaging Presentation

10/30/100/500

Regulatory Information

Prescription

Supporting Information

RANBAXY PHARMACEUTICALS CANADA INC.

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INDIA

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Virtual Booth

SOLIFENACIN SUCCINATE

Dosage Form

TABLET

Dosage Strength

10MG

Approval Date

Brand Name

RAN-SOLIFENACIN

Application Number

2437996

Packaging Presentation

10/30/100/500

Regulatory Information

Prescription

Supporting Information

SANDOZ CANADA INCORPORATED

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GERMANY

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Virtual Booth

SOLIFENACIN SUCCINATE

Dosage Form

TABLET

Dosage Strength

5MG

Approval Date

Brand Name

SANDOZ SOLIFENACIN

Application Number

2399032

Packaging Presentation

30/100

Regulatory Information

Prescription

Supporting Information

SANDOZ CANADA INCORPORATED

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GERMANY

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Virtual Booth

SOLIFENACIN SUCCINATE

Dosage Form

TABLET

Dosage Strength

10MG

Approval Date

Brand Name

SANDOZ SOLIFENACIN

Application Number

2399040

Packaging Presentation

30/100

Regulatory Information

Prescription

Supporting Information

SANIS HEALTH INC

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CANADA

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Virtual Booth

SOLIFENACIN SUCCINATE

Dosage Form

TABLET

Dosage Strength

5MG

Approval Date

Brand Name

SOLIFENACIN

Application Number

2458241

Packaging Presentation

(3X10)/100

Regulatory Information

Prescription

Supporting Information

SANIS HEALTH INC

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CANADA

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Virtual Booth

SOLIFENACIN SUCCINATE

Dosage Form

TABLET

Dosage Strength

10MG

Approval Date

Brand Name

SOLIFENACIN

Application Number

2458268

Packaging Presentation

(3X10)/100

Regulatory Information

Prescription

Supporting Information

TEVA CANADA LIMITED

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ISRAEL

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Virtual Booth

SOLIFENACIN SUCCINATE

Dosage Form

TABLET

Dosage Strength

5MG

Approval Date

Brand Name

TEVA-SOLIFENACIN

Application Number

2397900

Packaging Presentation

7/10/30/100

Regulatory Information

Prescription

Supporting Information

TEVA CANADA LIMITED

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ISRAEL

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Virtual Booth

SOLIFENACIN SUCCINATE

Dosage Form

TABLET

Dosage Strength

10MG

Approval Date

Brand Name

TEVA-SOLIFENACIN

Application Number

2397919

Packaging Presentation

7/10/30/100

Regulatory Information

Prescription

Supporting Information

MDA INC.

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Post An Enquiry

Virtual Booth

SOLIFENACIN SUCCINATE

Dosage Form

TABLET

Dosage Strength

5MG

Approval Date

Brand Name

SOLIFENACIN SUCCINATE TABLETS

Application Number

2448335

Packaging Presentation

30

Regulatory Information

Prescription

Supporting Information

MDA INC.

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Post An Enquiry

Virtual Booth

SOLIFENACIN SUCCINATE

Dosage Form

TABLET

Dosage Strength

10MG

Approval Date

Brand Name

SOLIFENACIN SUCCINATE TABLETS

Application Number

2448343

Packaging Presentation

30

Regulatory Information

Prescription

Approved Drug Products containing Solifenacin Succinate listed with Health Canada. Original Data : Health Canada Website

Dosage Form

Dosage Strength

Approval Date

Brand Name

Application Number

Packaging Presentation

Regulatory Information

Supporting Information

Dosage Form

Dosage Strength

Approval Date

Brand Name

Application Number

Packaging Presentation

Regulatory Information

Supporting Information

Dosage Form

Dosage Strength

Approval Date

Brand Name

Application Number

Packaging Presentation

Regulatory Information

Supporting Information

Dosage Form

Dosage Strength

Approval Date

Brand Name

Application Number

Packaging Presentation

Regulatory Information

Supporting Information

Dosage Form

Dosage Strength

Approval Date

Brand Name

Application Number

Packaging Presentation

Regulatory Information

Supporting Information

Dosage Form

Dosage Strength

Approval Date

Brand Name

Application Number

Packaging Presentation

Regulatory Information

Supporting Information

Dosage Form

Dosage Strength

Approval Date

Brand Name

Application Number

Packaging Presentation

Regulatory Information

Supporting Information

Dosage Form

Dosage Strength

Approval Date

Brand Name

Application Number

Packaging Presentation

Regulatory Information

Supporting Information

Dosage Form

Dosage Strength

Approval Date

Brand Name

Application Number

Packaging Presentation

Regulatory Information

Supporting Information

Dosage Form

Dosage Strength

Approval Date

Brand Name

Application Number

Packaging Presentation

Regulatory Information