prednicarbate

North America

Canada (2)
X
Product
Pack
Market
Pres.
Dosage
ATC
Company
DERMATOP EMOLLIENT CREAM 0.1% cream
Rx
topical
D07AC18
DERMATOP OINTMENT 0.1% oint
Rx
topical
D07AC18
Product
Pack
Reg. Nr.
Reg. Type
Reg. Date
Reg. Valid
Revocation
Company
DERMATOP EMOLLIENT CREAM 0.1% cream
02230642
DERMATOP OINTMENT 0.1% oint
02227517
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United States (4)
X
Product
Pack
Market
Pres.
Dosage
ATC
Company
DERMATOP oint
N
topical
D07AC18
DERMATOP E EMOLLIENT 0.1% cream
N
topical
D07AC18
PREDNICARBATE 0.1% oint
Y
Rx
topical
D07AC18
PREDNICARBATE 0.1% cream
N
topical
D07AC18
Product
Pack
Reg. Nr.
Reg. Type
Reg. Date
Reg. Valid
Revocation
Company
DERMATOP oint
19568/1
NDA
23-09-1991
DERMATOP E EMOLLIENT 0.1% cream
20279/1
NDA
29-10-1993
PREDNICARBATE 0.1% oint
77236/1
ANDA
09-03-2007
PREDNICARBATE 0.1% cream
77287/1
ANDA
19-09-2006
Would you like to in or out-license dossiers? Do you have Marketing Authorization to sell? Would you like to sell or aquire companies? This is the right place for you to find new business opportunities in the pharmaceutical industry.

Europe

Austria (0)
No result.
Belgium (0)
No result.
Bosnia and Herzegovina (0)
No result.
Croatia (0)
No result.
Czechia (0)
No result.
Denmark (0)
No result.
Finland (0)
No result.
Hungary (0)
No result.
Iceland (0)
No result.
Ireland (0)
No result.
Lithuania (0)
No result.
Malta (0)
No result.
Netherlands (0)
No result.
Norway (0)
No result.
Poland (0)
No result.
Romania (0)
No result.
Slovenia (2)
X
Product
Pack
Market
Pres.
Dosage
ATC
Company
DERMATOP oint
tuba 10 g mazila
tuba 50 g mazila
-
-
Rx
Rx
Dermalna uporaba
D07AC18
DERMATOP cream
tuba 10 g kreme (2,5mg/1g)
tuba 50 g kreme (2,5mg/1g)
-
-
Rx
Rx
Dermalna uporaba
D07AC18
Product
Pack
Reg. Nr.
Reg. Type
Reg. Date
Reg. Valid
Revocation
Company
DERMATOP oint
tuba 10 g mazila
tuba 50 g mazila
-
-
DERMATOP cream
tuba 10 g kreme (2,5mg/1g)
tuba 50 g kreme (2,5mg/1g)
-
-
Product
Pack
Ex-fact
Wholesale
Net retail
Gr. retail
Company
DERMATOP oint
tuba 10 g mazila
tuba 50 g mazila
DERMATOP cream
tuba 10 g kreme (2,5mg/1g)
tuba 50 g kreme (2,5mg/1g)
Would you like to in or out-license dossiers? Do you have Marketing Authorization to sell? Would you like to sell or aquire companies? This is the right place for you to find new business opportunities in the pharmaceutical industry.

Spain (8)
X
Product
Pack
Market
Pres.
Dosage
ATC
Company
BATMEN 2,5 MG/G oint
1 tube of 30 g
1 tube of 60 g
Y
Y
Rx
Rx
cut
D07AC18
BATMEN 2,5 MG/G cream
1 tube of 30 g
1 tube of 60 g
Y
Y
Rx
Rx
cut
D07AC18
BATMEN 2,5 MG/G UNGÜENTO oint
1 tube of 30 g
1 tube of 60 g
Y
Y
Rx
Rx
cut
D07AC18
BATMEN SOLUCION cut sol
1 bottle of 60 ml
1 bottle of 60 ml con aplicaddor
Y
Y
Rx
Rx
cut
D07AC18
PEITEL 2,5 MG/G cut sol
1 bottle of 60 ml
1 bottle of 60 ml con aplicaddor
Y
Y
Rx
Rx
cut
D07AC18
PEITEL 2,5 MG/G oint
1 tube of 30 g
1 tube of 60 g
Y
Y
Rx
Rx
cut
D07AC18
PEITEL 2,5 MG/G cream
1 tube of 30 g
1 tube of 60 g
Y
Y
Rx
Rx
cut
D07AC18
PEITEL 2,5 MG/G UNGUENTO oint
1 tube of 30 g
1 tube of 60 g
Y
Y
Rx
Rx
cut
D07AC18
Product
Pack
Reg. Nr.
Reg. Type
Reg. Date
Reg. Valid
Revocation
Company
BATMEN 2,5 MG/G oint
1 tube of 30 g
1 tube of 60 g
60456
60456
01-07-1996
01-07-1996
BATMEN 2,5 MG/G cream
1 tube of 30 g
1 tube of 60 g
60458
60458
01-07-1996
01-07-1996
BATMEN 2,5 MG/G UNGÜENTO oint
1 tube of 30 g
1 tube of 60 g
60457
60457
01-07-1996
01-07-1996
BATMEN SOLUCION cut sol
1 bottle of 60 ml
1 bottle of 60 ml con aplicaddor
60459
60459
01-07-1996
01-07-1996
PEITEL 2,5 MG/G cut sol
1 bottle of 60 ml
1 bottle of 60 ml con aplicaddor
60393
60393
01-12-1994
01-12-1994
PEITEL 2,5 MG/G oint
1 tube of 30 g
1 tube of 60 g
60370
60370
01-12-1994
01-12-1994
PEITEL 2,5 MG/G cream
1 tube of 30 g
1 tube of 60 g
60372
60372
01-12-1994
01-12-1994
PEITEL 2,5 MG/G UNGUENTO oint
1 tube of 30 g
1 tube of 60 g
60371
60371
01-12-1994
01-12-1994
Product
Pack
SPC
PIL
Company
BATMEN 2,5 MG/G oint
1 tube of 30 g
1 tube of 60 g
BATMEN 2,5 MG/G cream
1 tube of 30 g
1 tube of 60 g
BATMEN 2,5 MG/G UNGÜENTO oint
1 tube of 30 g
1 tube of 60 g
BATMEN SOLUCION cut sol
1 bottle of 60 ml
1 bottle of 60 ml con aplicaddor
PEITEL 2,5 MG/G cut sol
1 bottle of 60 ml
1 bottle of 60 ml con aplicaddor
PEITEL 2,5 MG/G oint
1 tube of 30 g
1 tube of 60 g
PEITEL 2,5 MG/G cream
1 tube of 30 g
1 tube of 60 g
PEITEL 2,5 MG/G UNGUENTO oint
1 tube of 30 g
1 tube of 60 g
Would you like to in or out-license dossiers? Do you have Marketing Authorization to sell? Would you like to sell or aquire companies? This is the right place for you to find new business opportunities in the pharmaceutical industry.

Sweden (2)
X
Product
Pack
Market
Pres.
Dosage
ATC
Company
PREDNIKARBAT GALEN 2,5 MG/G oint
Rx
-
D07AC18
PREDNIKARBAT GALEN 2,5 MG/G cream
Rx
Rx
-
D07AC18
Product
Pack
Reg. Nr.
Reg. Type
Reg. Date
Reg. Valid
Revocation
Company
PREDNIKARBAT GALEN 2,5 MG/G oint
Nationell decentral eller ömsesidig
26-05-2016
PREDNIKARBAT GALEN 2,5 MG/G cream
Nationell decentral eller ömsesidig
Nationell decentral eller ömsesidig
30-08-2012
24-09-2018
30-08-2015
Would you like to in or out-license dossiers? Do you have Marketing Authorization to sell? Would you like to sell or aquire companies? This is the right place for you to find new business opportunities in the pharmaceutical industry.

Switzerland (7)
X
Product
Pack
Market
Pres.
Dosage
ATC
Company
PREDNICUTAN oint
-
-
-
-
B
B
B
B
-
D07AC18
PREDNICUTAN Creme
-
-
-
-
B
B
B
B
-
D07AC18
PREDNICUTAN Fettsalbe
-
-
-
-
B
B
B
B
-
D07AC18
PREDNICUTAN CRINALE sol
-
-
-
B
B
B
-
D07AC18
PREDNITOP 0,25 % oint
-
B
-
D07AC18
PREDNITOP 0,25 % cream
-
B
-
D07AC18
PREDNITOP 0,25 % Lösung mit Schaumapplikator
-
B
-
D07AC18
Product
Pack
Reg. Nr.
Reg. Type
Reg. Date
Reg. Valid
Revocation
Company
PREDNICUTAN oint
60151 1
60151 1
60151 1
60151 1
Hauptzulassung
Hauptzulassung
Hauptzulassung
Hauptzulassung
18-11-2010
18-11-2010
18-11-2010
18-11-2010
PREDNICUTAN Creme
60153 1
60153 1
60153 1
60153 1
Hauptzulassung
Hauptzulassung
Hauptzulassung
Hauptzulassung
18-11-2010
18-11-2010
18-11-2010
18-11-2010
PREDNICUTAN Fettsalbe
60152 1
60152 1
60152 1
60152 1
Hauptzulassung
Hauptzulassung
Hauptzulassung
Hauptzulassung
18-11-2010
18-11-2010
18-11-2010
18-11-2010
PREDNICUTAN CRINALE sol
62322 1
62322 1
62322 1
Hauptzulassung
Hauptzulassung
Hauptzulassung
27-07-2012
27-07-2012
27-07-2012
26-07-2022
26-07-2022
26-07-2022
PREDNITOP 0,25 % oint
49679 2
Hauptzulassung
20-07-1990
15-02-2024
PREDNITOP 0,25 % cream
49676 2
Hauptzulassung
20-07-1990
15-02-2024
PREDNITOP 0,25 % Lösung mit Schaumapplikator
49678 1
Hauptzulassung
20-07-1990
15-02-2024
Would you like to in or out-license dossiers? Do you have Marketing Authorization to sell? Would you like to sell or aquire companies? This is the right place for you to find new business opportunities in the pharmaceutical industry.