All the information on this site is from our Global Pharmaceutical Database.
C07AA06
timolol
For informational purposes only, X-Pharma does not provide medical advice.
SPC/PIL of the products can differ from this general indication.
S01ED01SPC/PIL of the products can differ from this general indication.
C07AA06
North America
Canada (10)
X
United States (53)Product
Pack
Market
Pres.
Dosage
ATC
Company
Product
Pack
Reg. Nr.
Reg. Type
Reg. Date
Reg. Valid
Revocation
Company
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X
Product
Pack
Market
Pres.
Dosage
ATC
Company
Product
Pack
Reg. Nr.
Reg. Type
Reg. Date
Reg. Valid
Revocation
Company
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Europe
Austria (8)
X
Belgium (14)Product
Pack
Market
Pres.
Dosage
ATC
Company
Product
Pack
Reg. Nr.
Reg. Type
Reg. Date
Reg. Valid
Revocation
Company
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X
Croatia (3)Product
Pack
Market
Pres.
Dosage
ATC
Company
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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X
Czechia (5)Product
Pack
Market
Pres.
Dosage
ATC
Company
1 bočica 5 ml otopina
2 bočice 5 ml otopina
2 bočice 5 ml otopina
T
T
T
Rx
Rx
Rx
-
S01ED01
Product
Pack
Reg. Nr.
Reg. Type
Reg. Date
Reg. Valid
Revocation
Company
1 bočica nastavkom za kapanje 5 ml otopi
HR-H-890931943-01
25-04-2018
1 bočica nastavkom za kapanje 5 ml otopi
HR-H-663735137-01
25-04-2018
1 bočica 5 ml otopina
2 bočice 5 ml otopina
2 bočice 5 ml otopina
HR-H-980830974-01
HR-H-980830974-02
HR-H-980830974-02
18-03-2016
18-03-2016
18-03-2016
18-03-2021
18-03-2021
18-03-2021
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X
Denmark (14)Product
Pack
Market
Pres.
Dosage
ATC
Company
5MG/ML 1X10ML
5MG/ML 1X5ML
5MG/ML 3X5ML
5MG/ML 1X5ML
5MG/ML 3X5ML
Y
N
N
N
N
ocular
S01ED01
Product
Pack
Reg. Nr.
Reg. Type
Reg. Date
Reg. Valid
Revocation
Company
5MG/ML 1X10ML
5MG/ML 1X5ML
5MG/ML 3X5ML
5MG/ML 1X5ML
5MG/ML 3X5ML
64/ 247/00-C
64/ 247/00-C
64/ 247/00-C
64/ 247/00-C
64/ 247/00-C
NP
NP
NP
NP
NP
5MG/ML 1X5ML
5MG/ML 3X5ML
5MG/ML 3X5ML
64/ 069/97-C
64/ 069/97-C
64/ 069/97-C
NP
NP
NP
Product
Pack
Ex-fact
Wholesale
Net retail
Gr. retail
Company
5MG/ML 1X10ML
5MG/ML 1X5ML
5MG/ML 3X5ML
5MG/ML 1X5ML
5MG/ML 3X5ML
43,1
0
79,06
0
79,06
64,95
119,14
119,14
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X
Hungary (2)Product
Pack
Market
Pres.
Dosage
ATC
Company
Product
Pack
Reg. Nr.
Reg. Type
Reg. Date
Reg. Valid
Revocation
Company
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X
Iceland (3)Product
Pack
Market
Pres.
Dosage
ATC
Company
1x5ml cseppentős container hdpe cap
1x5ml cseppentős container pp cap
3x5ml cseppentős container hdpe cap
3x5ml cseppentős container pp cap
1x5ml cseppentős container pp cap
3x5ml cseppentős container hdpe cap
3x5ml cseppentős container pp cap
N
Y
N
N
Y
N
N
Rx
Rx
Rx
Rx
Rx
Rx
Rx
-
S01ED01
Product
Pack
Reg. Nr.
Reg. Type
Reg. Date
Reg. Valid
Revocation
Company
1x5ml cseppentős container hdpe cap
1x5ml cseppentős container pp cap
3x5ml cseppentős container hdpe cap
3x5ml cseppentős container pp cap
1x5ml cseppentős container pp cap
3x5ml cseppentős container hdpe cap
3x5ml cseppentős container pp cap
OGYI-T-01904/03
OGYI-T-01904/01
OGYI-T-01904/04
OGYI-T-01904/02
OGYI-T-01904/01
OGYI-T-01904/04
OGYI-T-01904/02
01-01-1992
01-01-1992
01-01-1992
01-01-1992
01-01-1992
01-01-1992
01-01-1992
Product
Pack
Ex-fact
Wholesale
Net retail
Gr. retail
Company
1x5ml cseppentős container hdpe cap
1x5ml cseppentős container pp cap
3x5ml cseppentős container hdpe cap
3x5ml cseppentős container pp cap
1x5ml cseppentős container pp cap
3x5ml cseppentős container hdpe cap
3x5ml cseppentős container pp cap
0
413
0
0
413
0
0
0
446,04
0
0
446,04
0
0
0
566
0
0
566
0
0
0
594
0
0
594
0
0
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X
Ireland (7)Product
Pack
Market
Pres.
Dosage
ATC
Company
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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X
Lithuania (11)Product
Pack
Market
Pres.
Dosage
ATC
Company
Product
Pack
Reg. Nr.
Reg. Type
Reg. Date
Reg. Valid
Revocation
Company
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X
Malta (14)Product
Pack
Market
Pres.
Dosage
ATC
Company
N30 single dose container
N90 single dose container
N90 single dose container
Rx
Rx
Rx
ocular
S01ED01
Product
Pack
Reg. Nr.
Reg. Type
Reg. Date
Reg. Valid
Revocation
Company
5 ml su dropper N1 bottle
LT/1/94/0364/001
NP
22-06-1994
5 ml su dropper N1 bottle
LT/1/94/0364/002
NP
22-06-1994
5 ml, su dropper N1 bottle
LT/1/95/2520/002
NP
05-04-1995
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X
Poland (5)Product
Pack
Market
Pres.
Dosage
ATC
Company
Product
Pack
Reg. Nr.
Reg. Type
Reg. Date
Reg. Valid
Revocation
Company
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.
X
Romania (6)Product
Pack
Market
Pres.
Dosage
ATC
Company
Product
Pack
Reg. Nr.
Reg. Type
Reg. Date
Reg. Valid
Revocation
Company
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.
X
Slovenia (16)Product
Pack
Market
Pres.
Dosage
ATC
Company
3 plicuri din hartie/Al x 10 recipiente
9 plicuri din hartie/Al x 10 recipiente
9 plicuri din hartie/Al x 10 recipiente
-
-
-
P6L
P6L
P6L
-
S01ED01
1 flac. din PEID prevazut cu pompa de vi
-
P6L
-
S01ED01
1 flac. PEJD, prevazut cu aplicator pt.
-
P6L
-
S01ED01
1 flac. PEJD, prevazut cu aplicator pt.
-
P6L
-
S01ED01
1 flac. din PEJD prevazut cu picurator d
-
P6L
-
S01ED01
1 flac. din PEJD prevazut cu picurator d
-
P6L
-
S01ED01
Product
Pack
Reg. Nr.
Reg. Type
Reg. Date
Reg. Valid
Revocation
Company
3 plicuri din hartie/Al x 10 recipiente
9 plicuri din hartie/Al x 10 recipiente
9 plicuri din hartie/Al x 10 recipiente
-
-
-
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X
Spain (10)Product
Pack
Market
Pres.
Dosage
ATC
Company
steklenička 2,5 ml (5mg/1ml)
steklenička 5 ml (5mg/1ml)
steklenička 5 ml (5mg/1ml)
-
-
-
Rx
Rx
Rx
ocular
S01ED01
plastičnim vsebnikom 5 ml sol in zaporko
N
Rx
ocular
S01ED01
belo prosojno kapalno plastenko iz LDPE
OCUMETER PLUS kapalno plastenko 2,5 ml s
OCUMETER PLUS kapalno plastenko 2,5 ml s
-
N
N
Rx
Rx
Rx
ocular
S01ED01
belo prosojno kapalno plastenko iz LDPE
OCUMETER PLUS kapalno plastenko 2,5 ml s
OCUMETER PLUS kapalno plastenko 2,5 ml s
-
N
N
Rx
Rx
Rx
ocular
S01ED01
Product
Pack
Reg. Nr.
Reg. Type
Reg. Date
Reg. Valid
Revocation
Company
kapalnim vsebnikom 5 g gela
5363-U-I-704/09
NP
20-08-2013
30-09-2013
30-03-2015
plastičnim vsebnikom 5 ml sol in zaporko
103-174-2014-3-U
NP
05-12-2016
21-10-2015
21-04-2017
plastičnim vsebnikom 5 ml sol in zaporko
103-174/2014-3-U
NP
05-12-2016
21-10-2015
21-04-2017
belo prosojno kapalno plastenko iz LDPE
OCUMETER PLUS kapalno plastenko 2,5 ml s
OCUMETER PLUS kapalno plastenko 2,5 ml s
10023-33/2018-9
103-27/2016-4
103-27/2016-4
NP
NP
NP
10-04-2019
16-09-2016
16-09-2016
belo prosojno kapalno plastenko iz LDPE
OCUMETER PLUS kapalno plastenko 2,5 ml s
OCUMETER PLUS kapalno plastenko 2,5 ml s
10023-33/2018-9
103-27/2016-4
103-27/2016-4
NP
NP
NP
10-04-2019
16-09-2016
16-09-2016
1 vsebnikom 5 ml sol
1010-149/2014-13
DCP
14-09-2016
14-09-2021
1 vsebnikom 5 ml sol
1010-149/2014-13
DCP
14-09-2016
14-09-2021
Product
Pack
Ex-fact
Wholesale
Net retail
Gr. retail
Company
kapalna plastenka 5 ml (2,5 mg/ml)
kapalna plastenka 5 ml (5 mg/ml)
steklenička 5 ml (2,5mg/1ml)
steklenička 2,5 ml (2,5mg/1ml)
steklenička 2,5 ml (5mg/1ml)
steklenička 5 ml (5mg/1ml)
steklenička 5 ml (5mg/1ml)
belo prosojno kapalno plastenko iz LDPE
OCUMETER PLUS kapalno plastenko 2,5 ml s
OCUMETER PLUS kapalno plastenko 2,5 ml s
6,27
6,27
6,27
belo prosojno kapalno plastenko iz LDPE
OCUMETER PLUS kapalno plastenko 2,5 ml s
OCUMETER PLUS kapalno plastenko 2,5 ml s
6,75
6,75
6,75
stekleničko 5 ml sol
stekleničko 5 ml sol
ALU kapalno plastenko 2,5 ml sol
ALU kapalno plastenko 2,5 ml sol
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X
Sweden (28)Product
Pack
Market
Pres.
Dosage
ATC
Company
Product
Pack
Reg. Nr.
Reg. Type
Reg. Date
Reg. Valid
Revocation
Company
1 bottle of 3 ml
1 bottle of 5 ml
1 bottle of 5 ml
55237
55237
55237
01-04-1980
01-04-1980
01-04-1980
1 bottle of 3 ml
1 bottle of 5 ml
1 bottle of 5 ml
55236
55236
55236
01-04-1980
01-04-1980
01-04-1980
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X
Switzerland (9)Product
Pack
Market
Pres.
Dosage
ATC
Company
Product
Pack
Reg. Nr.
Reg. Type
Reg. Date
Reg. Valid
Revocation
Company
Nationell decentral eller ömsesidig
28-04-1989
31-12-2009
Nationell decentral eller ömsesidig
15-12-1978
31-10-2008
Nationell decentral eller ömsesidig
02-05-1985
31-10-2008
Nationell decentral eller ömsesidig
15-12-1978
30-11-2012
Nationell decentral eller ömsesidig
02-05-1985
31-10-2008
Nationell decentral eller ömsesidig
10-09-1993
31-01-2018
Nationell decentral eller ömsesidig
10-09-1993
31-05-2018
Nationell decentral eller ömsesidig
11-09-1998
31-12-2016
Nationell decentral eller ömsesidig
11-09-1998
31-12-2016
Nationell decentral eller ömsesidig
09-12-1988
31-12-2017
Nationell decentral eller ömsesidig
09-12-1988
31-12-2017
PI
PI
PI
PI
PI
PI
PI
10-09-2012
05-10-2011
15-06-2011
10-09-2012
05-10-2011
15-06-2011
10-09-2012
10-09-2017
05-10-2016
31-01-2020
31-01-2020
05-10-2016
31-01-2020
31-01-2020
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X
Product
Pack
Market
Pres.
Dosage
ATC
Company
Product
Pack
Reg. Nr.
Reg. Type
Reg. Date
Reg. Valid
Revocation
Company
55788 1
55788 1
55788 1
55788 1
55788 1
55788 1
55788 1
Hauptzulassung
Hauptzulassung
Hauptzulassung
Hauptzulassung
Hauptzulassung
Hauptzulassung
Hauptzulassung
24-05-2002
24-05-2002
24-05-2002
24-05-2002
24-05-2002
24-05-2002
24-05-2002
07-05-2022
07-05-2022
07-05-2022
07-05-2022
07-05-2022
07-05-2022
07-05-2022
55788 2
55788 2
55788 2
55788 2
55788 2
55788 2
55788 2
Hauptzulassung
Hauptzulassung
Hauptzulassung
Hauptzulassung
Hauptzulassung
Hauptzulassung
Hauptzulassung
24-05-2002
24-05-2002
24-05-2002
24-05-2002
24-05-2002
24-05-2002
24-05-2002
07-05-2022
07-05-2022
07-05-2022
07-05-2022
07-05-2022
07-05-2022
07-05-2022
41634 2
41634 2
41634 2
41634 2
41634 2
41634 2
41634 2
Hauptzulassung
Hauptzulassung
Hauptzulassung
Hauptzulassung
Hauptzulassung
Hauptzulassung
Hauptzulassung
04-07-1978
04-07-1978
04-07-1978
04-07-1978
04-07-1978
04-07-1978
04-07-1978
12-11-2022
12-11-2022
12-11-2022
12-11-2022
12-11-2022
12-11-2022
12-11-2022
41634 3
41634 3
41634 3
41634 3
41634 3
41634 3
41634 3
Hauptzulassung
Hauptzulassung
Hauptzulassung
Hauptzulassung
Hauptzulassung
Hauptzulassung
Hauptzulassung
04-07-1978
04-07-1978
04-07-1978
04-07-1978
04-07-1978
04-07-1978
04-07-1978
12-11-2022
12-11-2022
12-11-2022
12-11-2022
12-11-2022
12-11-2022
12-11-2022
52509 1
52509 1
52509 1
52509 1
52509 1
52509 1
52509 1
Hauptzulassung
Hauptzulassung
Hauptzulassung
Hauptzulassung
Hauptzulassung
Hauptzulassung
Hauptzulassung
28-06-1994
28-06-1994
28-06-1994
28-06-1994
28-06-1994
28-06-1994
28-06-1994
24-11-2023
24-11-2023
24-11-2023
24-11-2023
24-11-2023
24-11-2023
24-11-2023
52509 2
52509 2
52509 2
52509 2
52509 2
52509 2
52509 2
Hauptzulassung
Hauptzulassung
Hauptzulassung
Hauptzulassung
Hauptzulassung
Hauptzulassung
Hauptzulassung
28-06-1994
28-06-1994
28-06-1994
28-06-1994
28-06-1994
28-06-1994
28-06-1994
24-11-2023
24-11-2023
24-11-2023
24-11-2023
24-11-2023
24-11-2023
24-11-2023
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