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

prednisolone

North America

Canada (7)
X
Product
Pack
Market
Pres.
Dosage
ATC
Company
Rx
OPHTHALMIC
S01BA04
Rx
OPHTHALMIC
S01BA04
Rx
OPHTHALMIC
S01BA04
Rx
OPHTHALMIC
S01BA04
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United States (0)
No result.

Europe

Austria (24)
X
Product
Pack
Reg. Nr.
Reg. Type
Reg. Date
Reg. Valid
Revocation
Company
1-24819
20-01-2003
14326
10-12-1969
13352
20-04-1979
10260
30-03-1965
10261
12-04-1965
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Belgium (1)
X
Product
Pack
Market
Pres.
Dosage
ATC
Company
5 mL
Y
ocular
S01BA04
Product
Pack
Reg. Nr.
Reg. Type
Reg. Date
Reg. Valid
Revocation
Company
Product
Pack
Ex-fact
Wholesale
Net retail
Gr. retail
Company
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Croatia (2)
X
Product
Pack
Market
Pres.
Dosage
ATC
Company
1 bočica sa 100 ml otopina i aplikator
Y
Rx
-
D07XA02
1 bočica sa 100 ml otopina i aplikator
Y
Rx
-
D07XA02
Product
Pack
Reg. Nr.
Reg. Type
Reg. Date
Reg. Valid
Revocation
Company
1 bočica sa 100 ml otopina i aplikator
HR-H-523824477-01
28-06-2017
1 bočica sa 100 ml otopina i aplikator
HR-H-105701584-01
28-06-2017
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Czechia (3)
X
Product
Pack
Market
Pres.
Dosage
ATC
Company
2MG/ML+4MG/ML 100ML
Y
cut
D07XA02
0,05MG/ML+2MG/ML+4MG/ML 1X100ML
Y
cut
D07XA02
5MG/ML 1X5ML
Y
ocular
S01BA04
Product
Pack
Reg. Nr.
Reg. Type
Reg. Date
Reg. Valid
Revocation
Company
2MG/ML+4MG/ML 100ML
46/ 150/94-C
NP
0,05MG/ML+2MG/ML+4MG/ML 1X100ML
46/ 151/94-C
NP
5MG/ML 1X5ML
64/ 071/97-C
NP
Product
Pack
Ex-fact
Wholesale
Net retail
Gr. retail
Company
2MG/ML+4MG/ML 100ML
225,8
336,95
0,05MG/ML+2MG/ML+4MG/ML 1X100ML
279,92
416,12
5MG/ML 1X5ML
57,74
87,01
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Denmark (14)
X
Product
Pack
Reg. Nr.
Reg. Type
Reg. Date
Reg. Valid
Revocation
Company
28105565015
DCP
07-04-2016
28105564815
DCP
07-04-2016
28105565115
DCP
07-04-2016
28105565215
DCP
07-04-2016
28105565315
DCP
07-04-2016
28105564915
DCP
07-04-2016
28100744276
NP
01-08-1977
28100838680
NP
19-05-1981
28100777276
NP
03-01-1978
28100230857
NP
04-06-1957
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Hungary (7)
X
Product
Pack
Market
Pres.
Dosage
ATC
Company
1x100ml glass
Y
Rx
topical
D07XA02
1x100ml glass
Y
Rx
topical
D07XA02
1x20g al tube
Y
Rx
topical
C05AA04
1x20g al tube
1x5g al tube
Y
N
Rx
Rx
topical
D07AA03
100x blister
20x blister
Y
Y
Rx
Rx
oral
H02AB06
1000 g
Y
Rx
-
H02AB06
10x5ml single-dose container
N
Rx
-
H02AB06
Product
Pack
Reg. Nr.
Reg. Type
Reg. Date
Reg. Valid
Revocation
Company
1x100ml glass
OGYI-T-06208/01
01-01-1998
1x100ml glass
OGYI-T-07461/01
08-06-2000
1x20g al tube
OGYI-T-03596/01
01-01-1982
1x20g al tube
1x5g al tube
OGYI-T-03189/02
OGYI-T-03189/01
18-05-1961
18-05-1961
100x blister
20x blister
OGYI-T-03091/03
OGYI-T-03091/01
01-01-1959
01-01-1959
1000 g
Ph. Hg. VIII.
10x5ml single-dose container
OGYI-T-23011/01
15-04-2016
08-04-2020
Product
Pack
Ex-fact
Wholesale
Net retail
Gr. retail
Company
1x100ml glass
0
0
0
0
1x100ml glass
0
0
0
0
1x20g al tube
0
0
0
0
1x20g al tube
1x5g al tube
591
0
631
0
776
0
815
0
100x blister
20x blister
1274
687
1339
731,66
1647
900
1729
945
1000 g
750000
900000
1260000
1323000
10x5ml single-dose container
0
0
0
0
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Iceland (6)
X
Product
Pack
Market
Pres.
Dosage
ATC
Company
Product
Pack
Reg. Nr.
Reg. Type
Reg. Date
Reg. Valid
Revocation
Company
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Ireland (19)
X
Product
Pack
Reg. Nr.
Reg. Type
Reg. Date
Reg. Valid
Revocation
Company
PPA1151/213/001
23-01-2015
PA22699/001/001
04-01-2013
PA22699/001/002
04-01-2013
PA1113/001/001
27-10-1978
PA0126/027/002
11-05-1988
PA22643/003/001
11-02-2011
PA1142/034/001
14-11-2014
PA0126/027/001
01-09-1982
PPA1151/123/002
30-10-2009
PA1025/011/002
01-04-1978
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Lithuania (6)
X
Product
Pack
Market
Pres.
Dosage
ATC
Company
100 ml su aplikatoriumi N1 bottle
Rx
cut
D07XA02
100 ml su aplikatoriumi N1 bottle
Rx
cut
D07XA02
100 ml (su aplikatoriumi) N1 bottle
Rx
cut
D07XA02
N30 blister
Rx
oral
H02AB06
N100 blister
Rx
oral
H02AB06
N20 blister
N30 bottle
Rx
Rx
oral
H02AB06
Product
Pack
Reg. Nr.
Reg. Type
Reg. Date
Reg. Valid
Revocation
Company
100 ml su aplikatoriumi N1 bottle
LT/1/95/2900/001
NP
04-10-1995
100 ml su aplikatoriumi N1 bottle
LT/L/19/1087/001
PI
25-10-2019
100 ml (su aplikatoriumi) N1 bottle
LT/L/19/1158/001
PI
31-12-2019
N30 blister
LT/1/94/1471/001
NP
05-05-1994
N100 blister
LT/1/94/1628/002
NP
22-06-1994
N20 blister
N30 bottle
LT/1/95/2752/002
LT/1/95/2752/001
NP
NP
04-10-1995
04-10-1995
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Malta (23)
X
Product
Pack
Reg. Nr.
Reg. Type
Reg. Date
Reg. Valid
Revocation
Company
AA084/06701
10-07-2008
MA628/17103
29-04-2016
MA628/17101
29-04-2016
MA628/17104
29-04-2016
MA628/17105
29-04-2016
MA628/17106
29-04-2016
AA702/00602
11-10-2018
MA628/17102
29-04-2016
AA729/23301
23-08-2019
MA154/02301
23-08-2006
MA154/02302
23-08-2006
AA1359/00902
07-11-2019
AA082/05401
19-06-2009
AA1359/00901
07-11-2019
AA082/05402
21-12-2010
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Poland (21)
X
Product
Pack
Market
Pres.
Dosage
ATC
Company
1 bottle 100 ml
Rp
-
D07XA02
1 bottle 100 ml
Rp
-
D07XA02
1 bottle 100 ml
1 bottle 100 ml
Rp
Rp
-
D07XA02
1 bottle 100 ml
Rp
-
D07XA02
1 bottle 100 ml
1 bottle 100 ml
Rp
Rp
-
D07XA02
1 bottle 100 ml
1 bottle 100 ml
Rp
Rp
-
D07XA02
1 bottle 100 ml
1 bottle 100 ml
Rp
Rp
-
D07XA02
20 tabs blister
20 tabs w fiolce
Rp
Rp
-
H02AB06
100 tabs
20 tabs
30 tabs
Rp
Rp
Rp
-
H02AB06
100 tabs
20 tabs
30 tabs
Rp
Rp
Rp
-
H02AB06
1 amp + rozp. 2 ml
3 amp + rozp. 2 ml
Rp
Rp
-
H02AB06
1 vial proszku + 1 amp rozp. 5 ml
3 vial proszku + 3 amp rozp. 5 ml
Rp
Rp
-
H02AB06
100 tabs
20 tabs
60 tabs
Rp
Rp
Rp
-
H02AB06
1 amp + rozp. 2 ml
3 amp + rozp. 2 ml
Rp
Rp
-
H02AB06
10 poj. 5 ml
Rp
-
H02AB06
Product
Pack
Reg. Nr.
Reg. Type
Reg. Date
Reg. Valid
Revocation
Company
1 bottle 100 ml
181/10
PI
14-10-2020
1 bottle 100 ml
1 bottle 100 ml
739/15
176/13
PI
PI
02-11-2020
11-04-2023
1 bottle 100 ml
640/15
PI
23-09-2020
1 bottle 100 ml
517/13
PI
03-12-2018
1 bottle 100 ml
1 bottle 100 ml
22/17
197/10
PI
PI
29-01-2022
15-11-2020
1 bottle 100 ml
1 bottle 100 ml
136/15
71/13
PI
PI
23-03-2020
01-02-2023
1 bottle 100 ml
1 bottle 100 ml
281/15
175/13
PI
PI
02-06-2020
11-04-2023
1 bottle 100 ml
61/17
PI
21-02-2022
1 bottle 100 ml
287/13
PI
21-06-2023
1 bottle 100 ml
389/19
PI
18-10-2024
20 tabs blister
20 tabs w fiolce
01707
01707
NP
NP
100 tabs
20 tabs
30 tabs
24451
24451
24451
NP
NP
NP
13-12-2022
13-12-2022
13-12-2022
1 vial + rozp. 10 ml
23483
NP
11-10-2021
100 tabs
20 tabs
30 tabs
24452
24452
24452
NP
NP
NP
13-12-2022
13-12-2022
13-12-2022
1 amp + rozp. 2 ml
3 amp + rozp. 2 ml
23480
23480
NP
NP
11-10-2021
11-10-2021
1 vial proszku + 1 amp rozp. 5 ml
3 vial proszku + 3 amp rozp. 5 ml
23482
23482
NP
NP
11-10-2021
11-10-2021
100 tabs
20 tabs
60 tabs
24450
24450
24450
NP
NP
NP
13-12-2022
13-12-2022
13-12-2022
1 amp + rozp. 2 ml
3 amp + rozp. 2 ml
23481
23481
NP
NP
11-10-2021
11-10-2021
10 poj. 5 ml
23374
MRP
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Romania (0)
No result.
Slovenia (13)
X
Product
Pack
Market
Pres.
Dosage
ATC
Company
steklenička 100 ml sol
-
Rx
Dermalna uporaba
D07XA02
steklenička 100 ml sol
-
Rx
Dermalna uporaba
D07XA02
40 tabs
-
-
H02AB06
100 tabs
N
-
H02AB06
3 amp powd in 3 amp 1 ml topila
-
-
H02AB06
kapalna plastenka 5 ml sol (5mg/1ml)
-
Rx
ocular
S01BA04
tubo 5 g mazila za oko (5mg/1g)
-
Rx
ocular
S01BA04
Product
Pack
Reg. Nr.
Reg. Type
Reg. Date
Reg. Valid
Revocation
Company
steklenička 100 ml sol
-
steklenička 100 ml sol
-
40 tabs
/
-
05-11-2009
05-11-2010
40 tabs
842-103/2019
-
11-03-2019
11-03-2020
100 tabs
842-70/2019
-
25-02-2019
25-02-2020
100 tabs
842-158/2019
-
05-04-2019
05-04-2020
10 tabs
/
-
11-02-2016
11-02-2017
40 tabs
842-11/2018
-
25-01-2018
25-01-2019
40 tabs
/
-
15-07-2010
15-07-2011
3 amp powd in 3 amp 1 ml topila
/
-
30-03-2017
30-03-2018
3 amp powd in 3 amp 1 ml vehikla
842-109/2018
-
26-03-2018
26-03-2019
kapalna plastenka 5 ml sol (5mg/1ml)
-
tubo 5 g mazila za oko (5mg/1g)
-
Product
Pack
Ex-fact
Wholesale
Net retail
Gr. retail
Company
steklenička 100 ml sol
steklenička 100 ml sol
kapalna plastenka 5 ml sol (5mg/1ml)
tubo 5 g mazila za oko (5mg/1g)
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Spain (4)
X
Product
Pack
Market
Pres.
Dosage
ATC
Company
1 tube of 30 g
Y
OTC
cut
D07XA02
1 bottle of 10 ml
Y
Rx
oral
H02AB06
1 bottle of 125 ml
Y
Rx
oral
H02AB06
1 bottle of 5 ml
Y
Rx
ocular
S01BA04
Product
Pack
Reg. Nr.
Reg. Type
Reg. Date
Reg. Valid
Revocation
Company
1 tube of 30 g
34746
01-10-1960
1 bottle of 10 ml
47546
01-03-1969
1 bottle of 125 ml
84003
03-04-2019
1 bottle of 5 ml
62038
01-03-1999
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Sweden (26)
X
Product
Pack
Market
Pres.
Dosage
ATC
Company
Product
Pack
Reg. Nr.
Reg. Type
Reg. Date
Reg. Valid
Revocation
Company
Nationell decentral eller ömsesidig
01-04-1960
Nationell decentral eller ömsesidig
31-10-1963
30-09-2014
Nationell decentral eller ömsesidig
02-06-2016
Nationell decentral eller ömsesidig
02-06-2016
Nationell decentral eller ömsesidig
02-06-2016
Nationell decentral eller ömsesidig
02-06-2016
Nationell decentral eller ömsesidig
01-03-2012
Nationell decentral eller ömsesidig
18-11-2011
Nationell decentral eller ömsesidig
18-11-2011
Nationell decentral eller ömsesidig
06-04-2018
Nationell decentral eller ömsesidig
05-06-2014
Nationell decentral eller ömsesidig
09-03-1984
Nationell decentral eller ömsesidig
31-08-1973
Nationell decentral eller ömsesidig
09-03-1984
Nationell decentral eller ömsesidig
08-05-2014
07-08-2018
Nationell decentral eller ömsesidig
19-10-2001
30-06-2008
Nationell decentral eller ömsesidig
06-03-2017
Nationell decentral eller ömsesidig
16-10-2014
16-10-2017
Nationell decentral eller ömsesidig
16-10-2014
16-10-2017
Nationell decentral eller ömsesidig
16-10-2014
16-10-2017
Nationell decentral eller ömsesidig
16-10-2014
16-10-2017
Nationell decentral eller ömsesidig
29-07-1965
Nationell decentral eller ömsesidig
29-07-1965
Nationell decentral eller ömsesidig
30-09-1958
Nationell decentral eller ömsesidig
18-10-1966
28-02-2009
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Switzerland (13)
X
Product
Pack
Market
Pres.
Dosage
ATC
Company
-
B
-
D07XA02
-
B
-
D07XA02
-
-
B
B
-
D07AA03
-
-
B
B
-
C05AA04
-
B
-
C05AA04
Product
Pack
Reg. Nr.
Reg. Type
Reg. Date
Reg. Valid
Revocation
Company
42684 2
Hauptzulassung
19-09-1980
01-11-2024
45860 1
Hauptzulassung
13-03-1984
22-02-2024
34057 1
Hauptzulassung
04-11-1968
10-07-2022
29348 2
29348 2
29348 2
Hauptzulassung
Hauptzulassung
Hauptzulassung
15-04-1975
15-04-1975
15-04-1975
28-03-2024
28-03-2024
28-03-2024
29348 1
29348 1
29348 1
Hauptzulassung
Hauptzulassung
Hauptzulassung
15-04-1975
15-04-1975
15-04-1975
28-03-2024
28-03-2024
28-03-2024
29348 3
29348 3
Hauptzulassung
Hauptzulassung
15-04-1975
15-04-1975
28-03-2024
28-03-2024
28830 1
28830 1
Hauptzulassung
Hauptzulassung
16-08-1962
16-08-1962
24137 1
24137 1
Hauptzulassung
Hauptzulassung
20-08-1958
20-08-1958
17-10-2024
17-10-2024
24138 1
Hauptzulassung
04-06-1958
17-10-2024
38840 2
38840 2
Hauptzulassung
Hauptzulassung
11-11-1975
11-11-1975
38840 1
38840 1
Hauptzulassung
Hauptzulassung
11-11-1975
11-11-1975
38840 3
38840 3
Hauptzulassung
Hauptzulassung
11-11-1975
11-11-1975
23477 1
Hauptzulassung
20-06-1957
10-07-2022
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