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01 1ACTAVIS GROUP PTC EHF
02 1AUROBINDO PHARMA ITALIA Srl
03 1Eugia Pharma (Malta) Limited
04 1HIKMA FARMACEUTICA S.A.
05 1HOSPIRA ITALIA Srl
06 1Labatec Pharma Sa
07 1MSD ITALIA Srl
08 1Mepha Pharma Ag
09 1RANBAXY ITALIA SpA
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01 2Imipenem Anhydrous; Cilastatin
02 7Imipenem; Cilastatin
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01 1Imipenem+Cilastatin+500500 Mg 1 Unit Parenteral Use
02 2Imipenem+Cilastatin+500500 Mg 10 Units Parenteral Use
03 1Imipenem+Cilastatin+500500 Mg 20Ml 1 Units Parenteral Use
04 1Imipenem+Cilastatin+500500 Mg 20Ml 5 Units Parenteral Use
05 1Imipenem+Cilastatin+500500 Mg 30Ml 1 Units Parenteral Use
06 1Powder For Concentrate For Solution For Infusion
07 1Powder For Solution For Infusion
08 1Solution For Injection
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01 6Italy
02 1Spain
03 2Switzerland
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01 1Imecitin
02 3Imipenem And Cilastatin
03 1Imipenem Cilastatin
04 1Imipenem-Cilastatin Labatec
05 1Imipenem-Cilastatin-Mepha iv
06 1Imipenem/Cilastatina Aurovitas
07 1Tienam
Regulatory Info :
Registration Country : Italy
Brand Name : Imipenem And Cilastatin
Dosage Form : Imipenem+Cilastatin+500500 Mg 10 Units Parenteral Use
Dosage Strength : 10 VIALS EV 500 mg + 500 mg
Packaging :
Approval Date :
Application Number :
Regulatory Info :
Registration Country : Italy
Regulatory Info :
Registration Country : Italy
Brand Name : Imecitin
Dosage Form : Imipenem+Cilastatin+500500 Mg 1 Unit Parenteral Use
Dosage Strength : 1 vial EV 500 mg + 500 mg
Packaging :
Approval Date :
Application Number :
Regulatory Info :
Registration Country : Italy
Regulatory Info : Authorized
Registration Country : Spain
Brand Name : Imipenem/Cilastatina Aurovitas
Dosage Form : Powder For Solution For Infusion
Dosage Strength : 500MG; 500 MG
Packaging :
Approval Date : 2011-02-02
Application Number : 72637
Regulatory Info : Authorized
Registration Country : Spain
Regulatory Info :
Registration Country : Italy
Brand Name : Imipenem And Cilastatin
Dosage Form : Imipenem+Cilastatin+500500 Mg 10 Units Parenteral Use
Dosage Strength : 10 vials soluz Chk 500 mg + 500 mg
Packaging :
Approval Date :
Application Number :
Regulatory Info :
Registration Country : Italy
Regulatory Info :
Registration Country : Italy
Brand Name : Imipenem Cilastatin
Dosage Form : Imipenem+Cilastatin+500500 Mg 20Ml 5 Units Parenteral Use
Dosage Strength : 5 VIALS EV 500 mg + 500 mg 20 ml
Packaging :
Approval Date :
Application Number :
Regulatory Info :
Registration Country : Italy
Regulatory Info : Allowed
Registration Country : Switzerland
Imipenem Anhydrous; Cilastatin
Brand Name : Imipenem-Cilastatin Labatec
Dosage Form : Solution For Injection
Dosage Strength :
Packaging :
Approval Date : 18/12/2009
Application Number : 59764
Regulatory Info : Allowed
Registration Country : Switzerland
Regulatory Info : Allowed
Registration Country : Switzerland
Imipenem Anhydrous; Cilastatin
Brand Name : Imipenem-Cilastatin-Mepha iv
Dosage Form : Powder For Concentrate For Solution For Infusion
Dosage Strength :
Packaging :
Approval Date : 24/06/2010
Application Number : 60262
Regulatory Info : Allowed
Registration Country : Switzerland
Regulatory Info :
Registration Country : Italy
Brand Name : Tienam
Dosage Form : Imipenem+Cilastatin+500500 Mg 20Ml 1 Units Parenteral Use
Dosage Strength : 1 vial soluz Chk 500 mg + 500 mg 20 ml
Packaging :
Approval Date :
Application Number :
Regulatory Info :
Registration Country : Italy
Regulatory Info :
Registration Country : Italy
Brand Name : Imipenem And Cilastatin
Dosage Form : Imipenem+Cilastatin+500500 Mg 30Ml 1 Units Parenteral Use
Dosage Strength : 1 vial EV 30 ml 500 mg + 500 mg
Packaging :
Approval Date :
Application Number :
Regulatory Info :
Registration Country : Italy