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01 1Amoxicillin
02 1Amoxicillin Sodium; Clavulanate Potassium
03 3Amoxicillin Trihydrate
04 2Amoxicillin; Clavulanic Acid
05 2Ampicillin Sodium
06 2Ampicillinnatrium
07 1Azithromycin Dihydrate
08 2Benzylpenicillin Potassium
09 1Clavulanate Potassium; Amoxicillin Trihydrate
10 2Clonazepam
11 1Diazepam
12 1Doxycycline
13 1Isoniazid; Rifampicin
14 1Potassium Citrate
15 1Rifampicin
16 1Rifampicin; Isoniazid
17 1Tetracycline
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01 4Film Coated Tablet
02 1Granule For Oral Suspension
03 3Hard Capsule
04 6Injection/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 31g
07 120MG/ML
08 1250MG
09 12MG
10 12g
11 13.1g
12 1300MG
13 1500MG
14 1500MG; 100MG
15 1500mg
16 15MG/ML
17 15ML
18 15millionIU
19 1750mg
20 180MG/ML; 11.4MG/ML
21 1875MG; 125MG
22 1Blank
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01 3Denmark
02 15Malta
03 6Sweden
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01 1Amotaks,
02 3Amotax
03 4Ampitar
04 1Azimycin
05 2Clonazepamum Tzf,
06 1Doxycyclinum Tzf,
07 1Nefrocitran
08 1Neorelium,
09 2Penicryl
10 2Rifamazid,
11 1Rifampicyna Tzf,
12 2Taromentin
13 1Taromentin,
14 1Taromentin, (400
15 1Tetracyclinum Tzf,
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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 : Prescription
Registration Country : Denmark
Dosage Form : Injection/Infusion Solution
Dosage Strength : 1g
Packaging :
Brand Name : Ampitar
Approval Date : 14-02-2023
Application Number : 28106664521
Regulatory Info : Prescription
Registration Country : Denmark

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Regulatory Info : Prescription
Registration Country : Denmark
Dosage Form : Injection/Infusion Solution
Dosage Strength : 2g
Packaging :
Brand Name : Ampitar
Approval Date : 14-02-2023
Application Number : 28106664721
Regulatory Info : Prescription
Registration Country : Denmark

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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 : 2.02E+13
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 : 2.02E+13
Regulatory Info : Approved
Registration Country : Sweden

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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 : 2.02E+13
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 : 2.02E+13
Regulatory Info : Approved
Registration Country : Sweden

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