All the information on this site is from our Global Pharmaceutical Database.

hydrocortisone

North America

Canada (27)
X
Product
Pack
Market
Pres.
Dosage
ATC
Company
Rx
rectal/topical
C05AA01
Rx
topical
D07AA02
Rx
topical
D07AA02
Rx
rectal/topical
C05AA01
Product
Pack
Reg. Nr.
Reg. Type
Reg. Date
Reg. Valid
Revocation
Company
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United States (0)
No result.

Europe

Austria (10)
X
Product
Pack
Reg. Nr.
Reg. Type
Reg. Date
Reg. Valid
Revocation
Company
EU/1/17/1260/001
09-02-2018
EU/1/17/1260/002
09-02-2018
EU/1/17/1260/003
09-02-2018
EU/1/17/1260/004
09-02-2018
1-18460
17-06-1988
7483
16-12-1953
EU/1/11/715/002,006-008
03-11-2011
EU/1/11/715/001,003-005
03-11-2011
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Belgium (20)
X
Product
Pack
Market
Pres.
Dosage
ATC
Company
0,5 mg
-
oral
H02AB09
1 mg
-
oral
H02AB09
2 mg
-
oral
H02AB09
5 mg
-
oral
H02AB09
20 g
Y
rectal
A07EA02
15 g
30 g
30 g
-
N
Y


cut
D07AA02
20 g
30 g
-
-

cut
D07AA02
20 g
30 g
Y
-

cut
D07AA02
1 kg
15 g
30 g
5 g
60 g
-
-
Y
-
-




cut
D07AA02
50x
50x
-
-

oral
H02AB09
50x
50x
-
-

oral
H02AB09
0,4 mL
0,4 mL
Y
-

ocular
S01BA02
Product
Pack
Reg. Nr.
Reg. Type
Reg. Date
Reg. Valid
Revocation
Company
0,5 mg
EU/1/17/1260/001
CP
1 mg
EU/1/17/1260/002
CP
2 mg
EU/1/17/1260/003
CP
5 mg
EU/1/17/1260/004
CP
15 g
30 g
30 g
BE155845
BE155845
BE155845
-
-
-
20 g
30 g
BE133016
BE133016
-
-
20 g
30 g
BE133007
BE133007
-
-
1 kg
15 g
30 g
5 g
60 g
BE511244
BE053392
BE053392
BE053392
BE053392
-
-
-
-
-
50x
50x
EU/1/11/715/008
EU/1/11/715/006
CP
CP
50x
50x
EU/1/11/715/005
EU/1/11/715/003
CP
CP
0,4 mL
0,4 mL
BE509173
BE509173
-
-
100 mg, 2 mL
100 mg, 2 mL
BE061311
BE061311
-
-
2 mL, 250 mg
2 mL, 250 mg
BE061451
BE061451
-
-
4 mL, 500 mg
4 mL, 500 mg
BE061476
BE061476
-
-
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Croatia (5)
X
Product
Pack
Market
Pres.
Dosage
ATC
Company
-
Rx
-
H02AB09
100 tabs u bočici
Y
Rx
-
H02AB09
-
Rx
-
H02AB09
10 jednodoznih spremnika u sachet
20 jednodoznih spremnika u sachet
30 jednodoznih spremnika u sachet
60 jednodoznih spremnika u sachet
Y
Y
Y
Y
Rx
Rx
Rx
Rx
-
S01BA02
1 bočica praškom u donjem dijelu i 2 ml
Y
Rx
-
H02AB09
Product
Pack
Reg. Nr.
Reg. Type
Reg. Date
Reg. Valid
Revocation
Company
100 tabs u bočici
HR-H-281556040-01
26-07-2018
10 jednodoznih spremnika u sachet
20 jednodoznih spremnika u sachet
30 jednodoznih spremnika u sachet
60 jednodoznih spremnika u sachet
HR-H-079548102-01
HR-H-079548102-02
HR-H-079548102-03
HR-H-079548102-04
30-03-2017
30-03-2017
30-03-2017
30-03-2017
30-03-2022
30-03-2022
30-03-2022
30-03-2022
1 bočica praškom u donjem dijelu i 2 ml
HR-H-226141869-01
06-09-2018
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Czechia (13)
X
Product
Pack
Market
Pres.
Dosage
ATC
Company
0,5MG 50
N
oral
H02AB09
1MG 50
N
oral
H02AB09
2MG 50
N
oral
H02AB09
5MG 50
N
oral
H02AB09
10MG 100
10MG 20
10MG 50
N
Y
N
oral
H02AB09
10MG/G 10G
Y
cut
D07AA02
100MG 1 I
100MG 1 II
100MG 10 I
100MG 10 II
100MG 20 I
100MG 20 II
N
Y
N
N
N
N
iv/im
H02AB09
20MG 100(2X50)
20MG 50
N
N
oral
H02AB09
5MG 100(2X50)
5MG 50
N
N
oral
H02AB09
3,35MG/ML 10(1X10)
3,35MG/ML 20(2X10)
3,35MG/ML 30(3X10)
3,35MG/ML 60(6X10)
N
N
Y
N
ocular
S01BA02
Product
Pack
Reg. Nr.
Reg. Type
Reg. Date
Reg. Valid
Revocation
Company
0,5MG 50
EU/1/17/1260/001
CP
1MG 50
EU/1/17/1260/002
CP
2MG 50
EU/1/17/1260/003
CP
5MG 50
EU/1/17/1260/004
CP
10MG 100
10MG 20
10MG 50
56/ 261/97-C
56/ 261/97-C
56/ 261/97-C
NP
NP
NP
10MG/G 10G
46/ 349/69-C
NP
100MG 1 I
100MG 1 II
100MG 10 I
100MG 10 II
100MG 20 I
100MG 20 II
56/ 690/10-C
56/ 690/10-C
56/ 690/10-C
56/ 690/10-C
56/ 690/10-C
56/ 690/10-C
NP
NP
NP
NP
NP
NP
20MG 100(2X50)
20MG 50
EU/1/11/715/006
EU/1/11/715/002
ORP
ORP
5MG 100(2X50)
5MG 50
EU/1/11/715/003
EU/1/11/715/001
ORP
ORP
3,35MG/ML 10(1X10)
3,35MG/ML 20(2X10)
3,35MG/ML 30(3X10)
3,35MG/ML 60(6X10)
64/ 480/14-C
64/ 480/14-C
64/ 480/14-C
64/ 480/14-C
MRP/DCP
MRP/DCP
MRP/DCP
MRP/DCP
Product
Pack
Ex-fact
Wholesale
Net retail
Gr. retail
Company
10MG 100
10MG 20
10MG 50
0
108,97
0
164,22
100MG 1 I
100MG 1 II
100MG 10 I
100MG 10 II
100MG 20 I
100MG 20 II
32,34
32,34
0
0
0
0
48,74
48,74
20MG 100(2X50)
20MG 50
0
0
5MG 100(2X50)
5MG 50
0
0
3,35MG/ML 10(1X10)
3,35MG/ML 20(2X10)
3,35MG/ML 30(3X10)
3,35MG/ML 60(6X10)
0
0
228,55
0
340,97
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Denmark (26)
X
Product
Pack
Market
Pres.
Dosage
ATC
Company
Product
Pack
Reg. Nr.
Reg. Type
Reg. Date
Reg. Valid
Revocation
Company
28106032217
PI
08-02-2018
28101034579
NP
04-06-1985
28104238407
MRP
26-05-2008
28105729816
NP
23-10-2017
28105729916
NP
23-10-2017
28105235713
DCP
17-12-2014
28103101499
NP
15-07-1999
28101315887
NP
30-06-1989
28104727210
CP
03-11-2011
28104727110
CP
03-11-2011
28104051006
PI
10-05-2007
28101903697
PI
14-10-1997
28106062318
PI
12-03-2018
28100385861
NP
15-10-1963
28105502014
DCP
03-04-2017
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Hungary (14)
X
Product
Pack
Market
Pres.
Dosage
ATC
Company
50x hdpe bottle
N
Rx
-
H02AB09
50x hdpe bottle
N
Rx
-
H02AB09
50x hdpe bottle
N
Rx
-
H02AB09
50x hdpe bottle
N
Rx
-
H02AB09
100x glass
100x hdpe container
Y
Y
Rx
Rx
oral
H02AB09
1x5g al tube
N
Rx
topical
D07AA02
1x20g al tube
1x5g al tube
N
N
Rx
Rx
topical
D07AA02
1x15g al tube
Y
Rx
-
D07AA02
100x container (2x50)
50x container
N
N
Rx
Rx
-
H02AB09
100x container (2x50)
50x container
N
N
Rx
Rx
-
H02AB09
1x25g tube
Y
Rx
topical
C05AA01
10x fóliacsík
Y
Rx
rectal
C05AA01
1x2ml act-o-vial
Y
Rx
parenteral
H02AB09
Product
Pack
Reg. Nr.
Reg. Type
Reg. Date
Reg. Valid
Revocation
Company
50x hdpe bottle
EU/1/17/1260/001
09-02-2018
50x hdpe bottle
EU/1/17/1260/002
09-02-2018
50x hdpe bottle
EU/1/17/1260/003
09-02-2018
50x hdpe bottle
EU/1/17/1260/004
09-02-2018
100x glass
100x hdpe container
OGYI-T-09856/01
OGYI-T-09856/02
11-11-2004
11-11-2004
1x5g al tube
OGYI-T-20463/01
16-11-2007
1x20g al tube
1x5g al tube
OGYI-T-20463/03
OGYI-T-20463/02
16-11-2007
16-11-2007
1x15g al tube
OGYI-T-22929/01
16-10-2015
100x container (2x50)
50x container
EU/1/11/715/006
EU/1/11/715/002
03-11-2011
03-11-2011
100x container (2x50)
50x container
EU/1/11/715/003
EU/1/11/715/001
1x25g tube
OGYI-T-07516/01
17-07-2000
10x fóliacsík
OGYI-T-07517/01
17-07-2000
1x2ml act-o-vial
OGYI-T-01859/01
01-01-1992
Product
Pack
Ex-fact
Wholesale
Net retail
Gr. retail
Company
100x glass
100x hdpe container
1522
1522
1598,1
1598,1
1943
1943
2040
2040
1x5g al tube
0
0
0
0
1x20g al tube
1x5g al tube
0
0
0
0
0
0
0
0
100x container (2x50)
50x container
0
0
0
0
0
0
0
0
100x container (2x50)
50x container
0
0
0
0
0
0
0
0
1x25g tube
0
0
0
0
10x fóliacsík
0
0
0
0
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Iceland (13)
X
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.

Ireland (22)
X
Product
Pack
Market
Pres.
Dosage
ATC
Company
-
Rx
oral
H02AB09
-
Rx
oral
H02AB09
-
Rx
oral
H02AB09
-
Rx
oral
H02AB09
Y
Rx
oral
H02AB09
Product
Pack
Reg. Nr.
Reg. Type
Reg. Date
Reg. Valid
Revocation
Company
EU/1/17/1260/001
09-02-2018
EU/1/17/1260/002
09-02-2018
EU/1/17/1260/003
09-02-2018
EU/1/17/1260/004
09-02-2018
PA22647/002/002
30-03-1990
PA1986/054/001
01-04-1978
PA1107/013/001
23-06-2017
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Lithuania (18)
X
Product
Pack
Market
Pres.
Dosage
ATC
Company
N50 bottle
Rx
oral
H02AB09
N50 bottle
Rx
oral
H02AB09
N50 bottle
Rx
oral
H02AB09
N50 bottle
Rx
oral
H02AB09
N100 bottle
Rx
oral
H02AB09
N100 blister
Rx
oral
H02AB09
N100 blister
Rx
oral
H02AB09
N200 blister
Rx
oral
H02AB09
N50 blister
Rx
oral
H02AB09
10 g, N1 tube
30 g, N1 tube
OTC/Rx
OTC/Rx
cut
D07AA02
5 ml, N1 vial
Rx
leisti aplink sąnarį;leisti į sąnarį
H02AB09
N30 nenurodyta
oral
H02AB09
N20 nenurodyta
oral
H02AB09
N180 nenurodyta
Rx
oral
H02AB09
N30 nenurodyta
N30 nenurodyta

oral
H02AB09
N100 (2 x 50) (sudėtinė) bottle
N50 bottle
Rx
Rx
oral
H02AB09
N100 (2 x 50) (sudėtinė) bottle
N50 bottle
Rx
Rx
oral
H02AB09
N10 blister
OTC
rectal
C05AA01
Product
Pack
Reg. Nr.
Reg. Type
Reg. Date
Reg. Valid
Revocation
Company
N50 bottle
EU/1/17/1260/001
CP
19-02-2018
N50 bottle
EU/1/17/1260/002
CP
19-02-2018
N50 bottle
EU/1/17/1260/003
CP
19-02-2018
N50 bottle
EU/1/17/1260/004
CP
19-02-2018
N100 bottle
Nominal
N100 blister
Nominal
03-10-2019
N100 blister
Nominal
N200 blister
Nominal
N50 blister
Nominal
10 g, N1 tube
30 g, N1 tube
LT/1/95/1147/002
LT/1/95/1147/001
NP
NP
04-10-1995
04-10-1995
5 ml, N1 vial
LT/1/94/1026/001
NP
22-06-1994
N30 nenurodyta
Nominal
N20 nenurodyta
Nominal
N180 nenurodyta
Nominal
N30 nenurodyta
N30 nenurodyta
Nominal
Nominal
N100 (2 x 50) (sudėtinė) bottle
N50 bottle
EU/1/11/715/006
EU/1/11/715/002
CP
CP
03-11-2011
03-11-2011
N100 (2 x 50) (sudėtinė) bottle
N50 bottle
EU/1/11/715/003
EU/1/11/715/001
CP
CP
03-11-2011
03-11-2011
N10 blister
LT/1/94/0007/004
NP
05-07-1994
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Malta (30)
X
Product
Pack
Market
Pres.
Dosage
ATC
Company
Product
Pack
Reg. Nr.
Reg. Type
Reg. Date
Reg. Valid
Revocation
Company
AA200/01301
26-02-2008
AA806/01401
14-11-2011
AA1187/03401
06-05-2019
AA770/07801
11-11-2015
AA561/00201
28-12-2012
AA729/08701
24-01-2012
AA561/00202
28-12-2012
AA1195/00101
28-03-2017
AA729/08702
25-01-2012
PI521/00801A
18-11-2005
MA1359/02101
24-11-2005
AA561/00203
19-05-2017
AA227/01101
11-11-2009
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Poland (21)
X
Product
Pack
Market
Pres.
Dosage
ATC
Company
1 tube 20 g
10 sachet 1 g
OTC
OTC
-
D07AA02
1 vial proszku + 1 amp rozp. 2 ml
Rp
-
H02AB09
1 tube 10 g
1 tube 15 g
1 tube 20 g
1 tube 25 g
1 tube 30 g
OTC
OTC
OTC
OTC
OTC
-
D07AA02
20 tabs blister
20 tabs container
Rp
Rp
-
H02AB09
1 tube 15 g
OTC
-
D07AA02
180 tabs
60 tabs
Rp
Rp
-
H02AB09
1 tube 15 g
OTC
-
D07AA02
100 tabs
150 tabs
300 tabs
50 tabs
EU/Rx/RxRx/7RxOTC/Rx/7
EU/Rx/RxRx/7RxOTC/Rx/8
-
H02AB09
100 tabs
150 tabs
300 tabs
50 tabs
EU/Rx/RxRx/7RxOTC/Rx/OTC
EU/Rx/RxRx/7RxOTC/Rx/OTC/Rx
-
H02AB09
10 poj. jednodawkowych
20 poj. jednodawkowych
30 poj. jednodawkowych
60 poj. jednodawkowych
Rp
Rp
Rp
Rp
-
S01BA02
Product
Pack
Reg. Nr.
Reg. Type
Reg. Date
Reg. Valid
Revocation
Company
1 tube 20 g
10 sachet 1 g
09853
09853
NP
NP
1 vial proszku + 1 amp rozp. 2 ml
25387
DCP
28-05-2024
1 tube 10 g
1 tube 15 g
1 tube 20 g
1 tube 25 g
1 tube 30 g
22896
22896
22896
22896
22896
NP
NP
NP
NP
NP
16-12-2020
16-12-2020
16-12-2020
16-12-2020
16-12-2020
20 tabs blister
20 tabs container
02827
02827
NP
NP
180 tabs
60 tabs
22402
22402
NP
NP
1 tube 15 g
24551
NP
13-02-2023
100 tabs
150 tabs
300 tabs
50 tabs
CP
CP
CP
CP
100 tabs
150 tabs
300 tabs
50 tabs
CP
CP
CP
CP
10 poj. jednodawkowych
20 poj. jednodawkowych
30 poj. jednodawkowych
60 poj. jednodawkowych
24253
24253
24253
24253
DCP
DCP
DCP
DCP
14-09-2022
14-09-2022
14-09-2022
14-09-2022
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Romania (13)
X
Product
Pack
Market
Pres.
Dosage
ATC
Company
1 tubee Al x 18 g ung.
-
P6L
-
C05AA01
1 folie termosudata PVC/PE x 6 supoz.
2 folii termosudate PVC/PE x 3 supoz.
2 folii termosudate PVC/PE x 6 supoz.
-
-
-
P6L
P6L
P6L
-
C05AA01
1 tubee Al x 20 g ung.
-
PRF
-
D07AA02
x 1 tubee Al x 20 g oint
x 1 tubee Al x 35 g oint
-
-
P-RF
P-RF
-
D07AA02
1 flac. din sticla, cu capacitatea de 5
-
PR
-
H02AB09
1 flac. din sticla, cu capacitatea de 20
-
PR
-
H02AB09
1 flac. din sticla incolora care contine
-
PR
-
H02AB09
1 flac. din sticla inchis cu dop din cau
10 flac. din sticla inchise cu dop din c
-
-
PRF
PRF
-
H02AB09
1 fiola din sticla incolora, cu capacita
5 fiole din sticla incolora, cu capacita
-
-
PRF
PRF
-
H02AB09
x 25 tabs diviz.
-
PRF
-
H02AB09
1 flac. din sticla incolora cu dop din c
-
PRF
-
H02AB09
x 1 tubee Al x 25 g cream
-
PRF
-
D07XA01
10 (1x10) flac. single dose PEID introdu
20 (2x10) flac. single dose PEID introdu
30 (3x10) flac. single dose PEID introdu
60 (6x10) flac. single dose PEID introdu
-
-
-
-
PRF
PRF
PRF
PRF
-
S01BA02
Product
Pack
Reg. Nr.
Reg. Type
Reg. Date
Reg. Valid
Revocation
Company
1 tubee Al x 18 g ung.
-
1 folie termosudata PVC/PE x 6 supoz.
2 folii termosudate PVC/PE x 3 supoz.
2 folii termosudate PVC/PE x 6 supoz.
-
-
-
1 tubee Al x 20 g ung.
-
x 1 tubee Al x 20 g oint
x 1 tubee Al x 35 g oint
-
-
1 flac. din sticla, cu capacitatea de 5
-
1 flac. din sticla, cu capacitatea de 20
-
1 flac. din sticla inchis cu dop din cau
10 flac. din sticla inchise cu dop din c
-
-
1 fiola din sticla incolora, cu capacita
5 fiole din sticla incolora, cu capacita
-
-
x 1 tubee Al x 25 g cream
-
10 (1x10) flac. single dose PEID introdu
20 (2x10) flac. single dose PEID introdu
30 (3x10) flac. single dose PEID introdu
60 (6x10) flac. single dose PEID introdu
-
-
-
-
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.

Slovenia (13)
X
Product
Pack
Market
Pres.
Dosage
ATC
Company
100 tabs
-
-
H02AB09
20 tabs (1 x 20 tabs blister)
-
Rx
oral
H02AB09
tuba 5 g mazila
-
-
S01BA02
20 tabs
50 tabs (5 x 10 tabs blister)
-
-

-
H02AB09
20 tabs 10 mg (2 x 10 tabs blister)
-
Rx
oral
H02AB09
20 tabs
-
-
H02AB09
tubo 15 g kreme (10 mg/g)
-
OTC
Dermalna uporaba
D07AA02
2 vrečicama, vsaka 10 enoodmernimi vsebn
3 vrečicami, vsaka 10 enoodmernimi vsebn
6 vrečicami, vsaka 10 enoodmernimi vsebn
-
N
-
Rx
Rx
Rx
ocular
S01BA02
1 dvodelno vial powd (Act-O-Vial) in 2 m
N
Rx
iv
H02AB09
1 dvodelno vial powd (Act-O-vial) in 4 m
N
Rx
iv
H02AB09
Product
Pack
Reg. Nr.
Reg. Type
Reg. Date
Reg. Valid
Revocation
Company
100 tabs
842-175/2019
-
15-04-2019
15-04-2020
20 tabs (1 x 20 tabs blister)
1000-16/2013-44
NP
19-12-2016
19-12-2021
20 tabs
/
-
06-04-2011
06-04-2016
20 tabs
50 tabs (5 x 10 tabs blister)
842-47/2019
4262-87/2012
-
-
06-02-2019
28-08-2012
06-02-2020
28-08-2013
20 tabs 10 mg (2 x 10 tabs blister)
-
25 tabs
842-239/2018
-
10-09-2018
10-09-2019
25 tabs
/
-
18-01-2013
18-01-2014
20 tabs
/
-
15-02-2011
15-02-2016
tubo 15 g kreme (10 mg/g)
-
2 vrečicama, vsaka 10 enoodmernimi vsebn
3 vrečicami, vsaka 10 enoodmernimi vsebn
6 vrečicami, vsaka 10 enoodmernimi vsebn
1010-156/2014-20
1010-156/2014-20
1010-156/2014-20
DCP
DCP
DCP
18-07-2017
18-07-2017
18-07-2017
18-07-2022
18-07-2022
18-07-2022
1 dvodelno vial powd (Act-O-Vial) in 2 m
5363-I-81/10
NP
06-01-2010
1 dvodelno vial powd (Act-O-vial) in 4 m
5363-I-82/10
NP
06-01-2010
Product
Pack
Ex-fact
Wholesale
Net retail
Gr. retail
Company
100 tabs
26,34
20 tabs (1 x 20 tabs blister)
1,52
20 tabs
50 tabs (5 x 10 tabs blister)
5,53
20 tabs 10 mg (2 x 10 tabs blister)
tubo 15 g kreme (10 mg/g)
2 vrečicama, vsaka 10 enoodmernimi vsebn
3 vrečicami, vsaka 10 enoodmernimi vsebn
6 vrečicami, vsaka 10 enoodmernimi vsebn
8,47
1 dvodelno vial powd (Act-O-Vial) in 2 m
2,05
1 dvodelno vial powd (Act-O-vial) in 4 m
6,99
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 (21)
X
Product
Pack
Market
Pres.
Dosage
ATC
Company
1 vial
10 vials
-
Y
Rx
Rx
VÍA INTRAARTICULAR, VÍA INTRAMUSCULAR, VÍA INTRAVENOSA, INFILTRACIÓN
H02AB09
1 vial + 1 amp of solv
10 vials + 10 amp of solv
-
-
Rx
Rx
VÍA INTRAVENOSA, VÍA INTRAMUSCULAR
H02AB09
1 vial + 1 amp of solv
10 vials
-
Y
Rx
Rx
iv/im
H02AB09
12 tabs
-
OTC
oral
A01AC03
1 tube of 30 g
Y
Rx
rectal
C05AA01
1 tube of 30 g
Y
OTC
cut
D07AA02
1 envase a presión of 50 g
Y
OTC
cut
D07AA02
1 tube of 30 g
1 tube of 60 g
Y
Y
OTC
OTC
rectal
C05AA01
1 tube of 30 g
Y
Rx
cut
D07AA02
1 tube of 15 g
1 tube of 30 g
Y
Y
OTC
OTC
rectal
C05AA01
1 tube of 30 g
1 tube of 60 g
Y
Y
OTC
OTC
rectal
C05AA01
10 tabs
30 tabs
-
Y
Rx
Rx
oral
H02AB09
1 tube of 30 g
1 tube of 50 g
Y
-
OTC
OTC
cut
D07AA02
1 envase a presión of 50 g
Y
OTC
cut
D07AA02
1 tube of 30 g
-
OTC
VÍA RECTAL, USO CUTÁNEO
C05AA01
1 bottle of 60 ml
Y
Rx
cut
D07AA02
1 bottle of 60 ml
-
Rx
cut
D07AA02
30 envases unidosis of 0,4 ml
Y
Rx
ocular
S01BA02
Product
Pack
Reg. Nr.
Reg. Type
Reg. Date
Reg. Valid
Revocation
Company
1 vial
10 vials
28824
28824
01-02-1958
01-02-1958
1 vial + 1 amp of solv
10 vials + 10 amp of solv
52106
52106
01-02-1974
01-02-1974
1 vial + 1 amp of solv
10 vials
52105
52105
01-02-1974
01-02-1974
12 tabs
34260
01-09-1960
1 tube of 30 g
48992
01-06-1970
1 tube of 30 g
60889
01-11-1995
1 envase a presión of 50 g
60888
01-11-1995
1 tube of 30 g
1 tube of 60 g
58975
58975
01-07-1992
01-07-1992
1 tube of 30 g
21428
01-06-1954
1 tube of 15 g
1 tube of 30 g
46022
46022
01-06-1968
01-06-1968
1 tube of 30 g
1 tube of 60 g
27941
27941
01-09-1957
01-09-1957
10 tabs
30 tabs
25699
25699
01-03-1956
01-03-1956
1 tube of 30 g
1 tube of 50 g
60891
60891
01-11-1995
01-11-1995
1 envase a presión of 50 g
60890
01-11-1995
1 tube of 30 g
64232
21-09-2001
1 bottle of 60 ml
59709
01-03-1993
1 bottle of 60 ml
59710
01-03-1993
30 envases unidosis of 0,4 ml
82398
11-09-2017
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 (46)
X
Product
Pack
Market
Pres.
Dosage
ATC
Company
Rx
Rx
Rx
Rx
Rx
-
A07EA02
OTC/Rx
-
D07XA01
OTC
-
D07AA02
OTC/Rx
-
C05AA01
Product
Pack
Reg. Nr.
Reg. Type
Reg. Date
Reg. Valid
Revocation
Company
PI
04-04-2018
31-01-2020
Nationell decentral eller ömsesidig
09-09-1994
30-04-2020
PI
PI
27-04-2006
30-01-2003
31-12-2007
31-01-2020
PI
PI
PI
PI
PI
25-03-2004
25-03-2004
13-10-2004
08-05-2006
13-10-2004
31-12-2018
PI
PI
PI
06-12-2007
10-12-2008
08-02-2006
31-01-2020
31-01-2020
31-01-2018
PI
PI
15-01-2009
30-11-2007
31-01-2020
31-01-2017
Nationell decentral eller ömsesidig
05-02-1982
Nationell decentral eller ömsesidig
29-01-1955
Nationell decentral eller ömsesidig
03-09-1982
31-05-2005
Nationell decentral eller ömsesidig
28-11-1955
Nationell decentral eller ömsesidig
27-05-1964
31-05-2005
Nationell decentral eller ömsesidig
24-05-2019
Nationell decentral eller ömsesidig
24-05-2019
Nationell decentral eller ömsesidig
16-10-2019
Nationell decentral eller ömsesidig
21-07-2006
Nationell decentral eller ömsesidig
17-10-2019
Nationell decentral eller ömsesidig
17-10-2019
Nationell decentral eller ömsesidig
06-02-2017
Nationell decentral eller ömsesidig
06-02-2017
Nationell decentral eller ömsesidig
12-12-2014
Nationell decentral eller ömsesidig
30-04-2004
Nationell decentral eller ömsesidig
21-12-1990
Nationell decentral eller ömsesidig
21-12-1990
Nationell decentral eller ömsesidig
16-09-1988
Nationell decentral eller ömsesidig
29-05-1962
31-05-2011
Nationell decentral eller ömsesidig
29-05-1962
31-05-2011
Nationell decentral eller ömsesidig
24-05-2017
Nationell decentral eller ömsesidig
23-03-2011
Nationell decentral eller ömsesidig
13-02-1958
Nationell decentral eller ömsesidig
10-02-1967
Nationell decentral eller ömsesidig
03-10-1980
31-07-2008
Nationell decentral eller ömsesidig
03-10-1980
30-04-2010
Nationell decentral eller ömsesidig
24-01-1969
Nationell decentral eller ömsesidig
24-01-1969
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 (13)
X
Product
Pack
Reg. Nr.
Reg. Type
Reg. Date
Reg. Valid
Revocation
Company
51784 1
Hauptzulassung
26-08-1991
25-10-2020
51785 1
Hauptzulassung
26-08-1991
25-10-2020
51464 1
Hauptzulassung
24-04-1992
21-12-2021
57970 1
57970 1
Hauptzulassung
Hauptzulassung
04-07-2008
04-07-2008
03-07-2023
03-07-2023
63125 1
Hauptzulassung
14-07-2014
13-07-2024
18979 1
18979 1
18979 1
Hauptzulassung
Hauptzulassung
Hauptzulassung
09-07-1953
09-07-1953
09-07-1953
07-06-2022
07-06-2022
07-06-2022
62068 2
Hauptzulassung
20-12-2012
19-12-2022
62068 1
Hauptzulassung
20-12-2012
19-12-2022
50135 1
Hauptzulassung
31-03-1989
18-12-2023
50137 1
Exportzulassung
31-03-1989
18-12-2023
23533 1
Hauptzulassung
24-07-1957
23533 2
Hauptzulassung
24-07-1957
56695 1
Hauptzulassung
08-04-2005
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.