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01 2AbbVie Inc
02 2Apotex Inc
03 2AstraZeneca
04 3Pfizer Inc
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01 1Ceftarolina Fosamil 600Mg 1 Unit Parenteral Use
02 1INJ
03 4POWDER;INTRAVENOUS
04 1Powder For Concentrate For Infusion Solution
05 1Powder For Concentrate For Solution For Infusion
06 1Powder to concentrate to the infusion fluid, resolution
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01 1Allowed
02 1Authorized
03 2DISCN
04 1Originator
05 2RX
06 2Blank
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01 2CEFTAROLINE FOSAMIL
02 2TEFLARO
03 3Zinforo
04 1Zinforo 600mg
05 1Zinforum
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01 1Italy
02 1Norway
03 1South Africa
04 1Spain
05 1Switzerland
06 4USA
Regulatory Info : RX
Registration Country : USA
Brand Name : TEFLARO
Dosage Form : POWDER;INTRAVENOUS
Dosage Strength : 400MG/VIAL
Packaging :
Approval Date : 2010-10-29
Application Number : 200327
Regulatory Info : RX
Registration Country : USA
Regulatory Info : RX
Registration Country : USA
Brand Name : TEFLARO
Dosage Form : POWDER;INTRAVENOUS
Dosage Strength : 600MG/VIAL
Packaging :
Approval Date : 2010-10-29
Application Number : 200327
Regulatory Info : RX
Registration Country : USA
Regulatory Info : DISCN
Registration Country : USA
Brand Name : CEFTAROLINE FOSAMIL
Dosage Form : POWDER;INTRAVENOUS
Dosage Strength : 400MG/VIAL
Packaging :
Approval Date : 2021-09-21
Application Number : 208075
Regulatory Info : DISCN
Registration Country : USA
Regulatory Info : DISCN
Registration Country : USA
Brand Name : CEFTAROLINE FOSAMIL
Dosage Form : POWDER;INTRAVENOUS
Dosage Strength : 600MG/VIAL
Packaging :
Approval Date : 2021-09-21
Application Number : 208075
Regulatory Info : DISCN
Registration Country : USA
Regulatory Info :
Registration Country : Italy
Brand Name : Zinforo
Dosage Form : Ceftarolina Fosamil 600Mg 1 Unit Parenteral Use
Dosage Strength : 10 VIALS EV 600 mg Groun
Packaging :
Approval Date :
Application Number :
Regulatory Info :
Registration Country : Italy
Regulatory Info :
Registration Country : Norway
Brand Name : Zinforo
Dosage Form : Powder to concentrate to the infusion fluid, resolution
Dosage Strength : 600 mg
Packaging : Hood glass
Approval Date :
Application Number :
Regulatory Info :
Registration Country : Norway
Regulatory Info : Allowed
Registration Country : Switzerland
Brand Name : Zinforo
Dosage Form : Powder For Concentrate For Solution For Infusion
Dosage Strength : 600mg
Packaging :
Approval Date : 29/08/2013
Application Number : 62672
Regulatory Info : Allowed
Registration Country : Switzerland
Regulatory Info : Originator
Registration Country : South Africa
Brand Name : Zinforo 600mg
Dosage Form : INJ
Dosage Strength : 600mg
Packaging : 20X10mg
Approval Date :
Application Number :
Regulatory Info : Originator
Registration Country : South Africa
Regulatory Info : Authorized
Registration Country : Spain
Brand Name : Zinforum
Dosage Form : Powder For Concentrate For Infusion Solution
Dosage Strength : 600MG
Packaging :
Approval Date : 2012-10-25
Application Number : 12785001
Regulatory Info : Authorized
Registration Country : Spain