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01 2Terbinafin Hydrochloride
02 1Terbinafine Hydrochloride
03 2Terbinafinhydrochloride
04 1Terbinafinhydroklorid
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01 5Cutaneous Solution
02 1Liniment
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01 198MG
02 598mg/ml
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01 2Denmark
02 1Norway
03 1Spain
04 2Sweden
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01 1Terbinafin "Moberg Pharma"
02 2Terbinafine Moberg Pharma
03 3Terclara
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Regulatory Info : Approved
Registration Country : Sweden
Dosage Form : Cutaneous Solution
Dosage Strength : 98mg/ml
Packaging :
Brand Name : Terbinafine Moberg Pharma
Approval Date : 01/08/2023
Application Number : 20220325000057
Regulatory Info : Approved
Registration Country : Sweden

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Regulatory Info : Approved
Registration Country : Sweden
Dosage Form : Cutaneous Solution
Dosage Strength : 98mg/ml
Packaging :
Brand Name : Terclara
Approval Date : 02/08/2023
Application Number : 20220325000064
Regulatory Info : Approved
Registration Country : Sweden

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Regulatory Info : Marketed
Registration Country : Norway
Dosage Form : Liniment
Dosage Strength : 98mg/ml
Packaging :
Brand Name : Terclara
Approval Date :
Application Number :
Regulatory Info : Marketed
Registration Country : Norway

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Regulatory Info : Authorized
Registration Country : Spain
Dosage Form : Cutaneous Solution
Dosage Strength : 98MG
Packaging :
Brand Name : Terbinafine Moberg Pharma
Approval Date : 24-10-2023
Application Number : 89103
Regulatory Info : Authorized
Registration Country : Spain

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Regulatory Info : Prescription
Registration Country : Denmark
Dosage Form : Cutaneous Solution
Dosage Strength : 98mg/ml
Packaging :
Brand Name : Terbinafin \"Moberg Pharma\"
Approval Date : 08-08-2023
Application Number : 28106763722
Regulatory Info : Prescription
Registration Country : Denmark

Boost your online visibility by uploading your products, APIs, FDFs, intermediates, excipients, and services for free on PharmaCompass.
Rank higher among suppliers and expand your reach across the internet efficiently and cost-effectively.
Regulatory Info : Prescription
Registration Country : Denmark
Dosage Form : Cutaneous Solution
Dosage Strength : 98mg/ml
Packaging :
Brand Name : Terclara
Approval Date : 08-08-2023
Application Number : 28106763822
Regulatory Info : Prescription
Registration Country : Denmark
