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01 2Cefonicid Disodium
02 3Ciprofloxacin Hydrochloride (Monohydrate)
03 1Colextran
04 1Estradiol
05 1Levodropropizine
06 1Pantoprazole Sodium
07 3Terazosin
08 1Tranexamic acid
09 1Triamcinolone Acetonide; Framycetin Sulfate; Centella Asiatica Exto
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01 5ROTTAPHARM SPA
02 6Rottapharm Sl
03 3Rottapharm Spa
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01 1Capsule
02 1Cream
03 1Divisible Tablet
04 1Gastro-Resistant Tablet
05 3Modified Release Tablet
06 1Oral Drop
07 1Powder And Solvent For Injectable Solution
08 1Powder And Solvent For Injectable Solution And Infusion
09 1Solution For Injection For
10 2Tablets
11 1Transdermal Patches
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01 21000MG
02 12 mg
03 125 micrograms/24 hours
04 140MG
05 15 mg
06 1500 mg/5 ml
07 1500MG
08 3500mg
09 15mg
10 160MG
11 1Blank
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01 5Italy
02 6Spain
03 3Sweden
Regulatory Info : Cancelled
Registration Country : Spain
Dosage Form : Powder And Solvent For I...
Brand Name : Monocide
Dosage Strength : 1000MG
Packaging :
Approval Date : 1985-08-01
Application Number : 56628
Regulatory Info : Cancelled
Registration Country : Spain
Regulatory Info : Cancelled
Registration Country : Spain
Dosage Form : Powder And Solvent For I...
Brand Name : Monocide
Dosage Strength : 1000MG
Packaging :
Approval Date : 1985-08-01
Application Number : 56627
Regulatory Info : Cancelled
Registration Country : Spain
Regulatory Info : Deregistered
Registration Country : Sweden
Ciprofloxacin Hydrochloride (Monohydrate)
Dosage Form : Modified Release Tablet
Brand Name : Prorilis
Dosage Strength : 500mg
Packaging :
Approval Date : 03/07/2008
Application Number : 20060318000011
Regulatory Info : Deregistered
Registration Country : Sweden
Regulatory Info : Deregistered
Registration Country : Sweden
Ciprofloxacin Hydrochloride (Monohydrate)
Dosage Form : Modified Release Tablet
Brand Name : Urinary
Dosage Strength : 500mg
Packaging :
Approval Date : 03/07/2008
Application Number : 20060318000035
Regulatory Info : Deregistered
Registration Country : Sweden
Regulatory Info : Deregistered
Registration Country : Sweden
Ciprofloxacin Hydrochloride (Monohydrate)
Dosage Form : Modified Release Tablet
Brand Name : Utiminx
Dosage Strength : 500mg
Packaging :
Approval Date : 03/07/2008
Application Number : 20060318000028
Regulatory Info : Deregistered
Registration Country : Sweden
Regulatory Info : Cancelled
Registration Country : Spain
Dosage Form : Capsule
Brand Name : Dexide
Dosage Strength : 500MG
Packaging :
Approval Date : 1985-03-01
Application Number : 56430
Regulatory Info : Cancelled
Registration Country : Spain
Regulatory Info :
Registration Country : Italy
Dosage Form : Transdermal Patches
Brand Name : DERMESTRIL
Dosage Strength : 25 micrograms/24 hours
Packaging : 8 UNITS 25 MCG/DIE - TRANSDERMAL PATCHES
Approval Date :
Application Number :
Regulatory Info :
Registration Country : Italy
Regulatory Info : Cancelled
Registration Country : Spain
Dosage Form : Oral Drop
Brand Name : Levotuss
Dosage Strength : 60MG
Packaging :
Approval Date : 1995-02-01
Application Number : 60115
Regulatory Info : Cancelled
Registration Country : Spain
Regulatory Info : Cancelled
Registration Country : Spain
Dosage Form : Gastro-Resistant Tablet
Brand Name : Pantoprazole Madaus
Dosage Strength : 40MG
Packaging :
Approval Date : 2006-10-09
Application Number : 68075
Regulatory Info : Cancelled
Registration Country : Spain
Regulatory Info :
Registration Country : Italy
Dosage Form : Tablets
Brand Name : TERAFLUX
Dosage Strength : 5 mg
Packaging : 14 UNIT 5 MG - ORAL USE
Approval Date :
Application Number :
Regulatory Info :
Registration Country : Italy