01 6Bracco
02 1Haleon
03 2Pierre Fabre
04 1Teknomek
01 1Dry Sub C Solv
02 1FOR SUSPENSION;INTRAVENOUS
03 1Ophthalmic Gas
04 1POWDER AND SOLVENT FOR SOLUTION FOR INJECTION
05 1POWDER FOR SUSPENSION
06 1POWDER;TOPICAL
07 1Powder and liquid to the injection fluid, Dispersion
08 2Solution
09 1Sulfur Hexafluoride, 8Mcl/Ml 5Ml 1 Units Parenteral Use
01 1DISCN
02 1Ethical
03 1RX
04 7Blank
01 1BENSULFOID
02 2Ektoselen medicinal shampoo
03 1LUMASON
04 1SONOVUE
05 2SonoVue
06 2Sonovue
07 1Blank
01 1Canada
02 1Italy
03 1Norway
04 1Sweden
05 3Switzerland
06 1Turkey
07 2USA
Regulatory Info : RX
Registration Country : USA
SULFUR HEXAFLUORIDE LIPID-TYPE A MICROSPHERES
Brand Name : LUMASON
Dosage Form : FOR SUSPENSION;INTRAVENOUS
Dosage Strength : 60.7MG/25MG
Packaging :
Approval Date : 2014-10-15
Application Number : 203684
Regulatory Info : RX
Registration Country : USA
Regulatory Info :
Registration Country : Sweden
Brand Name : SonoVue
Dosage Form : POWDER AND SOLVENT FOR SOLUTION FOR INJECTION
Dosage Strength : 8 MICROL / ML
Packaging :
Approval Date :
Application Number :
Regulatory Info :
Registration Country : Sweden
Regulatory Info :
Registration Country : Italy
Brand Name : Sonovue
Dosage Form : Sulfur Hexafluoride, 8Mcl/Ml 5Ml 1 Units Parenteral Use
Dosage Strength : 8 mcl/ml 1 vial + 1 syringe 5 ml + Adapter
Packaging :
Approval Date :
Application Number :
Regulatory Info :
Registration Country : Italy
Regulatory Info :
Registration Country : Norway
Brand Name : SonoVue
Dosage Form : Powder and liquid to the injection fluid, Dispersion
Dosage Strength : 8 micro liters/ml
Packaging : Set
Approval Date :
Application Number :
Regulatory Info :
Registration Country : Norway
Regulatory Info :
Registration Country : Switzerland
Brand Name : Sonovue
Dosage Form : Dry Sub C Solv
Dosage Strength :
Packaging :
Approval Date :
Application Number :
Regulatory Info :
Registration Country : Switzerland
Regulatory Info : Ethical
Registration Country : Canada
Brand Name : SONOVUE
Dosage Form : POWDER FOR SUSPENSION
Dosage Strength : 8MCL/ML
Packaging :
Approval Date :
Application Number : 2287684
Regulatory Info : Ethical
Registration Country : Canada
Regulatory Info : DISCN
Registration Country : USA
Brand Name : BENSULFOID
Dosage Form : POWDER;TOPICAL
Dosage Strength : 33.32%
Packaging :
Approval Date : 1982-01-01
Application Number : 2918
Regulatory Info : DISCN
Registration Country : USA
Regulatory Info :
Registration Country : Switzerland
Brand Name : Ektoselen medicinal shampoo
Dosage Form : Solution
Dosage Strength :
Packaging :
Approval Date :
Application Number :
Regulatory Info :
Registration Country : Switzerland
Regulatory Info :
Registration Country : Switzerland
Brand Name : Ektoselen medicinal shampoo
Dosage Form : Solution
Dosage Strength :
Packaging :
Approval Date :
Application Number :
Regulatory Info :
Registration Country : Switzerland
Regulatory Info :
Registration Country : Turkey
Brand Name :
Dosage Form : Ophthalmic Gas
Dosage Strength : 10ML
Packaging :
Approval Date :
Application Number :
Regulatory Info :
Registration Country : Turkey
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