Sanofi is a pioneer in Diabetes Solutions, Human Vaccines, Innovative Drugs, Consumer Healthcare, and the new Genzyme.
01 1Sanofi
02 3A. Menarini
03 3Bausch Health
04 4Dermapharm Holding
05 1Ferrer Internacional
06 2Fougera Pharmaceuticals Inc.
07 3Galenicum
08 3Galenpharma Gmbh
09 2Kolmar Korea Co., Ltd.
10 1Seoul Pharma Co Ltd
01 2CREAM
02 2CREAM;TOPICAL
03 6Cream
04 1Cutaneous Solution
05 1Lotion
06 2OINTMENT;TOPICAL
07 6Ointment
08 1Prednicarbate 0.25% 30G Ointment Dermatological Use
09 1Salve
10 1Solution
01 4Allowed
02 1Approved
03 6Authorized
04 1Cancelled
05 3DISCN
06 2Deregistered
07 1Generic
08 1Prescription
09 1RX
10 3Blank
01 1Atop
02 3Batman
03 1DERMATOP
04 1DERMATOP E EMOLLIENT
05 1DERMATOP EMOLLIENT CREAM
06 2PREDNICARBATE
07 4Peitel
08 1Predna Cream
09 1Predna Lotion
10 3Prednicarbate Crazy
11 3Prednicutan
12 1Prednicutan Crinale
13 1SILCADE
01 1Canada
02 1Italy
03 3South Korea
04 7Spain
05 3Sweden
06 4Switzerland
07 4USA
Sanofi is a pioneer in Diabetes Solutions, Human Vaccines, Innovative Drugs, Consumer Healthcare, and the new Genzyme.
Regulatory Info :
Registration Country : Italy
Brand Name : Atop
Dosage Form : Prednicarbate 0.25% 30G Ointment Dermatological Use
Dosage Strength : cream derm 30 g 0.25%
Packaging :
Approval Date :
Application Number :
Regulatory Info :
Registration Country : Italy
Regulatory Info : Authorized
Registration Country : Spain
Brand Name : Batman
Dosage Form : Ointment
Dosage Strength : 2.5MG
Packaging :
Approval Date : 1996-07-01
Application Number : 60457
Regulatory Info : Authorized
Registration Country : Spain
Regulatory Info : Authorized
Registration Country : Spain
Brand Name : Batman
Dosage Form : Cream
Dosage Strength : 2.5MG
Packaging :
Approval Date : 1996-07-01
Application Number : 60458
Regulatory Info : Authorized
Registration Country : Spain
Regulatory Info : DISCN
Registration Country : USA
Brand Name : DERMATOP
Dosage Form : OINTMENT;TOPICAL
Dosage Strength : 0.1% **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons**
Packaging :
Approval Date : 1991-09-23
Application Number : 19568
Regulatory Info : DISCN
Registration Country : USA
Regulatory Info : DISCN
Registration Country : USA
Brand Name : DERMATOP E EMOLLIENT
Dosage Form : CREAM;TOPICAL
Dosage Strength : 0.1% **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons**
Packaging :
Approval Date : 1993-10-29
Application Number : 20279
Regulatory Info : DISCN
Registration Country : USA
Regulatory Info : Prescription
Registration Country : Canada
Brand Name : DERMATOP EMOLLIENT CREAM
Dosage Form : CREAM
Dosage Strength : 0.1%/W/W
Packaging :
Approval Date :
Application Number : 2230642
Regulatory Info : Prescription
Registration Country : Canada
Regulatory Info : Allowed
Registration Country : Switzerland
Brand Name : Prednicutan
Dosage Form : Ointment
Dosage Strength : 2.5mg
Packaging :
Approval Date : 18/11/2010
Application Number : 60151
Regulatory Info : Allowed
Registration Country : Switzerland
Regulatory Info : Allowed
Registration Country : Switzerland
Brand Name : Prednicutan
Dosage Form : Ointment
Dosage Strength : 2.5mg
Packaging :
Approval Date : 18/11/2010
Application Number : 60152
Regulatory Info : Allowed
Registration Country : Switzerland
Regulatory Info : Allowed
Registration Country : Switzerland
Brand Name : Prednicutan
Dosage Form : Cream
Dosage Strength : 2.5mg
Packaging :
Approval Date : 18/11/2010
Application Number : 60153
Regulatory Info : Allowed
Registration Country : Switzerland
Regulatory Info : Allowed
Registration Country : Switzerland
Brand Name : Prednicutan Crinale
Dosage Form : Solution
Dosage Strength : 2.5mg
Packaging :
Approval Date : 27/07/2012
Application Number : 62322
Regulatory Info : Allowed
Registration Country : Switzerland
Regulatory Info : RX
Registration Country : USA
Brand Name : PREDNICARBATE
Dosage Form : OINTMENT;TOPICAL
Dosage Strength : 0.1%
Packaging :
Approval Date : 2007-03-09
Application Number : 77236
Regulatory Info : RX
Registration Country : USA
Regulatory Info : DISCN
Registration Country : USA
Brand Name : PREDNICARBATE
Dosage Form : CREAM;TOPICAL
Dosage Strength : 0.1%
Packaging :
Approval Date : 2006-09-19
Application Number : 77287
Regulatory Info : DISCN
Registration Country : USA
Regulatory Info : Authorized
Registration Country : Spain
Brand Name : Peitel
Dosage Form : Cutaneous Solution
Dosage Strength : 2.5MG
Packaging :
Approval Date : 1994-12-01
Application Number : 60393
Regulatory Info : Authorized
Registration Country : Spain
Regulatory Info : Authorized
Registration Country : Spain
Brand Name : Peitel
Dosage Form : Ointment
Dosage Strength : 2.5MG
Packaging :
Approval Date : 1994-12-01
Application Number : 60370
Regulatory Info : Authorized
Registration Country : Spain
Regulatory Info :
Registration Country : South Korea
Brand Name : Predna Lotion
Dosage Form : Lotion
Dosage Strength : 0.25%
Packaging :
Approval Date :
Application Number :
Regulatory Info :
Registration Country : South Korea
Regulatory Info :
Registration Country : South Korea
Brand Name : Predna Cream
Dosage Form : Cream
Dosage Strength : 0.25%
Packaging :
Approval Date :
Application Number :
Regulatory Info :
Registration Country : South Korea
Regulatory Info : Generic
Registration Country : South Korea
Brand Name : SILCADE
Dosage Form : CREAM
Dosage Strength : 2.5MG/1G
Packaging :
Approval Date :
Application Number :
Regulatory Info : Generic
Registration Country : South Korea
Regulatory Info : Approved
Registration Country : Sweden
Brand Name : Prednicarbate Crazy
Dosage Form : Salve
Dosage Strength : 2.5mg/g
Packaging :
Approval Date : 26/05/2016
Application Number : 20150221000090
Regulatory Info : Approved
Registration Country : Sweden
Portfolio PDF
Product Web Link
Virtual Booth
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Website
Corporate PDF
Regulatory Info : Deregistered
Registration Country : Sweden
Brand Name : Prednicarbate Crazy
Dosage Form : Cream
Dosage Strength : 2.5mg/g
Packaging :
Approval Date : 24/09/2018
Application Number : 20170201000094
Regulatory Info : Deregistered
Registration Country : Sweden
Portfolio PDF
Product Web Link
Virtual Booth
Digital Content
Website
Corporate PDF
Regulatory Info : Deregistered
Registration Country : Sweden
Brand Name : Prednicarbate Crazy
Dosage Form : Cream
Dosage Strength : 2.5mg/g
Packaging :
Approval Date : 30/08/2012
Application Number : 20100314000018
Regulatory Info : Deregistered
Registration Country : Sweden
Portfolio PDF
Product Web Link
Virtual Booth
Digital Content
Website
Corporate PDF
