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01 2Associated Biotech
02 2Health Biotech
03 4K24 Pharmaceuticals
04 3Reyoung pharmaceutical
05 3Sandoz B2B
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01 1Amoxicillin 1.000Mg 100 Unita' Parenteral Use
02 1Amoxicillin 1.000Mg 50 Joined The Parenteral Use
03 1Amoxicillin 500Mg 100 Unita' Parenteral Use
04 1Amoxicillin 500Mg 50 Joined The Parenteral Use
05 2Dry Powder Injectable
06 3POWDER FOR SOLUTION
07 3Powder for Injection
08 2Tablet
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01 3Prescription
02 11Blank
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01 3AMOXICILLIN SODIUM AND POTASSIUM CLAVULANATE FOR INJECTION
02 2Amoxicillin Sodium
03 4Amoxillina Sodium
04 5Blank
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01 3Canada
02 3China
03 4India
04 4Italy
Regulatory Info :
Registration Country : India
Brand Name : Amoxicillin Sodium
Dosage Form : Dry Powder Injectable
Dosage Strength : 500MG
Packaging : 10ml, 20ml
Approval Date :
Application Number :
Regulatory Info :
Registration Country : India
Regulatory Info :
Registration Country : India
Brand Name : Amoxicillin Sodium
Dosage Form : Dry Powder Injectable
Dosage Strength : 1GM
Packaging : 10ml, 20ml
Approval Date :
Application Number :
Regulatory Info :
Registration Country : India
Regulatory Info :
Registration Country : India
Amoxicillin Sodium; Clavulanic Acid
Brand Name :
Dosage Form : Tablet
Dosage Strength : 875MG; 125MG
Packaging :
Approval Date :
Application Number :
Regulatory Info :
Registration Country : India
Regulatory Info :
Registration Country : India
Amoxicillin Sodium; Clavulanic Acid
Brand Name :
Dosage Form : Tablet
Dosage Strength : 500MG; 125MG
Packaging :
Approval Date :
Application Number :
Regulatory Info :
Registration Country : India
Regulatory Info :
Registration Country : Italy
Brand Name : Amoxillina Sodium
Dosage Form : Amoxicillin 1.000Mg 100 Unita' Parenteral Use
Dosage Strength : 100 bottles EV 1,000 mg
Packaging :
Approval Date :
Application Number :
Regulatory Info :
Registration Country : Italy
Regulatory Info :
Registration Country : Italy
Brand Name : Amoxillina Sodium
Dosage Form : Amoxicillin 1.000Mg 50 Joined The Parenteral Use
Dosage Strength : 50 bottles EV 1,000 mg
Packaging :
Approval Date :
Application Number :
Regulatory Info :
Registration Country : Italy
Regulatory Info :
Registration Country : Italy
Brand Name : Amoxillina Sodium
Dosage Form : Amoxicillin 500Mg 100 Unita' Parenteral Use
Dosage Strength : 100 bottles EV 500 mg
Packaging :
Approval Date :
Application Number :
Regulatory Info :
Registration Country : Italy
Regulatory Info :
Registration Country : Italy
Brand Name : Amoxillina Sodium
Dosage Form : Amoxicillin 500Mg 50 Joined The Parenteral Use
Dosage Strength : 50 bottles EV 500 mg
Packaging :
Approval Date :
Application Number :
Regulatory Info :
Registration Country : Italy
Regulatory Info :
Registration Country : China
Brand Name :
Dosage Form : Powder for Injection
Dosage Strength : 0.25g
Packaging :
Approval Date :
Application Number :
Regulatory Info :
Registration Country : China
Regulatory Info :
Registration Country : China
Brand Name :
Dosage Form : Powder for Injection
Dosage Strength : 0.5g
Packaging :
Approval Date :
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Regulatory Info :
Registration Country : China
Regulatory Info :
Registration Country : China
Brand Name :
Dosage Form : Powder for Injection
Dosage Strength : 1g
Packaging :
Approval Date :
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Regulatory Info :
Registration Country : China
Regulatory Info : Prescription
Registration Country : Canada
Brand Name : AMOXICILLIN SODIUM AND POTASSIUM CLAVULANATE FOR INJECTION
Dosage Form : POWDER FOR SOLUTION
Dosage Strength : 500MG/VIAL
Packaging :
Approval Date :
Application Number : 2495910
Regulatory Info : Prescription
Registration Country : Canada
Regulatory Info : Prescription
Registration Country : Canada
Brand Name : AMOXICILLIN SODIUM AND POTASSIUM CLAVULANATE FOR INJECTION
Dosage Form : POWDER FOR SOLUTION
Dosage Strength : 1000MG/VIAL
Packaging :
Approval Date :
Application Number : 2495929
Regulatory Info : Prescription
Registration Country : Canada
Regulatory Info : Prescription
Registration Country : Canada
Brand Name : AMOXICILLIN SODIUM AND POTASSIUM CLAVULANATE FOR INJECTION
Dosage Form : POWDER FOR SOLUTION
Dosage Strength : 2000MG/VIAL
Packaging :
Approval Date :
Application Number : 2495937
Regulatory Info : Prescription
Registration Country : Canada