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01 1Amoxicillin
02 1Amoxicillin Sodium; Clavulanate Potassium
03 3Amoxicillin Trihydrate
04 2Amoxicillin; Clavulanic Acid
05 2Ampicillinnatrium
06 1Azithromycin Dihydrate
07 1Benzylpenicillin Potassium
08 1Clavulanate Potassium; Amoxicillin Trihydrate
09 2Clonazepam
10 1Diazepam
11 1Doxycycline
12 1Isoniazid; Rifampicin
13 1Potassium Citrate
14 1Rifampicin
15 1Rifampicin; Isoniazid
16 1Tetracycline
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01 4Film Coated Tablet
02 1Granule For Oral Suspension
03 3Hard Capsule
04 3Injection/Infusion Solution
05 1Modified Release Tablet
06 1Powder For Oral Suspension
07 1Powder For Solution For Injection And Infusion
08 1Solution For Infusion
09 1Solution For Injection
10 5Tablet
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01 10.5MG
02 11080MG
03 1125MG; 875MG
04 1150MG; 10MG
05 1150MG; 300MG
06 21g
07 120MG/ML
08 1250MG
09 12MG
10 1300MG
11 1500MG
12 1500MG; 100MG
13 1500mg
14 15MG/ML
15 15ML
16 15millionIU
17 1750mg
18 180MG/ML; 11.4MG/ML
19 1875MG; 125MG
20 1Blank
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01 15Malta
02 6Sweden
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01 1Amotaks,
02 3Amotax
03 2Ampitar
04 1Azimycin
05 2Clonazepamum Tzf,
06 1Doxycyclinum Tzf,
07 1Nefrocitran
08 1Neorelium,
09 1Penicryl
10 2Rifamazid,
11 1Rifampicyna Tzf,
12 2Taromentin
13 1Taromentin,
14 1Taromentin, (400
15 1Tetracyclinum Tzf,
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Regulatory Info : Approved
Registration Country : Sweden
Dosage Form : Tablet
Dosage Strength : 1g
Packaging :
Brand Name : Amotax
Approval Date : 14/10/2024
Application Number : 20240821000030
Regulatory Info : Approved
Registration Country : Sweden

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Regulatory Info : Approved
Registration Country : Sweden
Dosage Form : Tablet
Dosage Strength : 500mg
Packaging :
Brand Name : Amotax
Approval Date : 14/10/2024
Application Number : 20240821000016
Regulatory Info : Approved
Registration Country : Sweden

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Regulatory Info : Approved
Registration Country : Sweden
Dosage Form : Tablet
Dosage Strength : 750mg
Packaging :
Brand Name : Amotax
Approval Date : 14/10/2024
Application Number : 20240821000023
Regulatory Info : Approved
Registration Country : Sweden

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Regulatory Info : Approved
Registration Country : Sweden
Dosage Form : Injection/Infusion Solution
Dosage Strength : 1g
Packaging :
Brand Name : Ampitar
Approval Date : 19/01/2023
Application Number : 20210825000015
Regulatory Info : Approved
Registration Country : Sweden

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Regulatory Info : Approved
Registration Country : Sweden
Dosage Form : Injection/Infusion Solution
Dosage Strength :
Packaging :
Brand Name : Ampitar
Approval Date : 19/01/2023
Application Number : 20210825000022
Regulatory Info : Approved
Registration Country : Sweden

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Regulatory Info : Authorised
Registration Country : Malta
Dosage Form : Granule For Oral Suspension
Dosage Strength : 5ML
Packaging :
Brand Name : Amotaks,
Approval Date : 2023-01-17
Application Number :
Regulatory Info : Authorised
Registration Country : Malta

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Regulatory Info : Authorised
Registration Country : Malta
Dosage Form : Film Coated Tablet
Dosage Strength : 875MG; 125MG
Packaging :
Brand Name : Taromentin
Approval Date : 2022-09-12
Application Number :
Regulatory Info : Authorised
Registration Country : Malta

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Regulatory Info : Authorised
Registration Country : Malta
Dosage Form : Powder For Oral Suspension
Dosage Strength : 80MG/ML; 11.4MG/ML
Packaging :
Brand Name : Taromentin, (400
Approval Date : 2022-12-22
Application Number :
Regulatory Info : Authorised
Registration Country : Malta

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Regulatory Info : Authorised
Registration Country : Malta
Amoxicillin Sodium; Clavulanate Potassium
Dosage Form : Powder For Solution For Inject...
Dosage Strength : 500MG; 100MG
Packaging :
Brand Name : Taromentin,
Approval Date : 2025-03-18
Application Number :
Regulatory Info : Authorised
Registration Country : Malta

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Regulatory Info : Authorised
Registration Country : Malta
Dosage Form : Film Coated Tablet
Dosage Strength : 500MG
Packaging :
Brand Name : Azimycin
Approval Date : 2020-09-30
Application Number :
Regulatory Info : Authorised
Registration Country : Malta

Polfa Tarchomin is a supplier offers 4 products (APIs, Excipients or Intermediates).
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