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01 4ESLICARBAZEPINE ACETATE
02 1ESZOPICLONE
03 4LURASIDONE HYDROCHLORIDE
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01 9TABLET
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01 11MG
02 1200MG
03 120MG
04 1400MG
05 140MG
06 1600MG
07 160MG
08 1800MG
09 180MG
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01 4APTIOM
02 4LATUDA
03 1LUNESTA
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Regulatory Info : PRESCRIPTION
Registration Country : Canada
Dosage Form : TABLET
Dosage Strength : 40MG
Packaging :
Brand Name : LATUDA
Approval Date :
Application Number : 2387751
Regulatory Info : PRESCRIPTION
Registration Country : Canada

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Regulatory Info : PRESCRIPTION
Registration Country : Canada
Dosage Form : TABLET
Dosage Strength : 80MG
Packaging :
Brand Name : LATUDA
Approval Date :
Application Number : 2387778
Regulatory Info : PRESCRIPTION
Registration Country : Canada

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Regulatory Info : PRESCRIPTION
Registration Country : Canada
Dosage Form : TABLET
Dosage Strength : 60MG
Packaging :
Brand Name : LATUDA
Approval Date :
Application Number : 2413361
Regulatory Info : PRESCRIPTION
Registration Country : Canada

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Regulatory Info : PRESCRIPTION
Registration Country : Canada
Dosage Form : TABLET
Dosage Strength : 20MG
Packaging :
Brand Name : LATUDA
Approval Date :
Application Number : 2422050
Regulatory Info : PRESCRIPTION
Registration Country : Canada

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Regulatory Info : PRESCRIPTION
Registration Country : Canada
Dosage Form : TABLET
Dosage Strength : 200MG
Packaging :
Brand Name : APTIOM
Approval Date :
Application Number : 2426862
Regulatory Info : PRESCRIPTION
Registration Country : Canada

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Regulatory Info : PRESCRIPTION
Registration Country : Canada
Dosage Form : TABLET
Dosage Strength : 400MG
Packaging :
Brand Name : APTIOM
Approval Date :
Application Number : 2426870
Regulatory Info : PRESCRIPTION
Registration Country : Canada

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Regulatory Info : PRESCRIPTION
Registration Country : Canada
Dosage Form : TABLET
Dosage Strength : 600MG
Packaging :
Brand Name : APTIOM
Approval Date :
Application Number : 2426889
Regulatory Info : PRESCRIPTION
Registration Country : Canada

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Regulatory Info : PRESCRIPTION
Registration Country : Canada
Dosage Form : TABLET
Dosage Strength : 800MG
Packaging :
Brand Name : APTIOM
Approval Date :
Application Number : 2426897
Regulatory Info : PRESCRIPTION
Registration Country : Canada

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Regulatory Info : PRESCRIPTION
Registration Country : Canada
Dosage Form : TABLET
Dosage Strength : 1MG
Packaging :
Brand Name : LUNESTA
Approval Date :
Application Number : 2453207
Regulatory Info : PRESCRIPTION
Registration Country : Canada

Sumitomo Pharma is a supplier offers 16 products (APIs, Excipients or Intermediates).
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