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

chlorhexidine

North America

Canada (39)
X
Product
Pack
Market
Pres.
Dosage
ATC
Company
OTC
topical
D08AC02
OTC
topical
D08AC02
OTC
topical
D08AC02
OTC
topical
D08AC02
OTC
topical
D08AC02
OTC
topical
D08AC02
OTC
topical
D08AC02
OTC
topical
D08AC02
OTC
topical
D08AC02
Product
Pack
Reg. Nr.
Reg. Type
Reg. Date
Reg. Valid
Revocation
Company
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United States (46)
X
Product
Pack
Market
Pres.
Dosage
ATC
Company
Y
OTC
topical
D09AA12
Y
OTC
topical
D08AC02
Y
OTC
topical
D08AC02
Y
OTC
topical
D08AC02
Y
OTC
topical
D08AC02
Y
OTC
topical
D08AC02
N
topical
D09AA12
Y
OTC
topical
D08AC02
Y
OTC
topical
D08AC02
Y
Rx
dental
A01AB03
Y
Rx
dental
A01AB03
Y
Rx
dental
A01AB03
Y
Y
Rx
Rx
dental
A01AB03
N
topical
D08AC02
Product
Pack
Reg. Nr.
Reg. Type
Reg. Date
Reg. Valid
Revocation
Company
19822/1
NDA
31-03-1989
71419/1
ANDA
17-12-1987
19258/2
NDA
22-07-1986
19258/1
NDA
22-07-1986
73416/1
ANDA
14-03-2000
19421/1
NDA
17-12-1985
19422/1
NDA
17-12-1985
19125/1
NDA
24-12-1984
18423/1
NDA
01-01-1982
17768/1
NDA
01-01-1982
18300/1
NDA
01-01-1982
72255/1
ANDA
15-04-1991
72295/1
ANDA
28-02-1991
76434/1
ANDA
29-11-2005
19028/1
NDA
13-08-1986
20774/1
NDA
15-05-1998
203212/1
73695/1
ANDA
ANDA
28-01-2016
14-01-1994
72292/1
ANDA
28-01-1992
70104/1
ANDA
24-07-1986
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Europe

Austria (10)
X
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Belgium (23)
X
Product
Pack
Market
Pres.
Dosage
ATC
Company
30 mL
N
oropharyngeal
A01AB03
12x
36x
40x
48x
-
Y
-
-



oropharyngeal
R02AA05
10 mL
10 mL
100 mL
15 mL
15 mL
25 mL
45 mL
45 mL
5 mL
Y
-
-
Y
-
-
Y
-
-








cut
D08AC02
50 g
Y
dental/gingival/oromucosal
A01AB03
200 mL
200 mL
Y
-

oromucosal
A01AB03
200 mL
200 mL
90 mL
90 mL
-
Y
-
-



oropharyngeal/oromucosal
A01AB03
20x
40x
-
-

oropharyngeal
R02AA05
100 mL
15 mL
50 mL
-
Y
Y


cut
D08AC02
125 mL
25 mL
25 mL
250 mL
5 L
500 mL
500 mL
Y
N
Y
Y
Y
Y
Y






cut
D08AC02
20 g
N
cut
D08AC02
24x
N
oropharyngeal
D08AC02
1x, 100 mL
1x, 300 mL
1x, 500 mL
50 mL
5000 mL
-
-
-
-
-




oromucosal
A01AB03
30x
Y
oropharyngeal
A01AB03
Product
Pack
Reg. Nr.
Reg. Type
Reg. Date
Reg. Valid
Revocation
Company
12x
36x
40x
48x
BE464773
BE464773
BE464773
BE464773
-
-
-
-
10 mL
10 mL
100 mL
15 mL
15 mL
25 mL
45 mL
45 mL
5 mL
BE400863
BE400863
BE400863
BE400863
BE400863
BE400863
BE400863
BE400863
BE400811
-
-
-
-
-
-
-
-
-
200 mL
200 mL
BE106802
BE106802
-
-
200 mL
200 mL
90 mL
90 mL
BE262157
BE177116
BE262157
BE177116
-
-
-
-
20x
40x
BE157832
BE157832
-
-
100 mL
15 mL
50 mL
BE118045
BE118045
BE118045
-
-
-
125 mL
25 mL
25 mL
250 mL
5 L
500 mL
500 mL
BE372075
BE078671
BE078671
BE372075
BE372075
BE372075
BE372075
-
-
-
-
-
-
-
5 L
500 mL
BE078741
BE078741
-
-
12x
36x
40x
48x
BE464782
BE464782
BE464782
BE464782
-
-
-
-
12x
36x
40x
48x
BE464791
BE464791
BE464791
BE464791
-
-
-
-
1x, 100 mL
1x, 300 mL
1x, 500 mL
50 mL
5000 mL
BE515182
BE515182
BE515182
BE515182
BE515182
-
-
-
-
-
30x
BE162014
-
Product
Pack
Ex-fact
Wholesale
Net retail
Gr. retail
Company
10 mL
10 mL
100 mL
15 mL
15 mL
25 mL
45 mL
45 mL
5 mL
200 mL
200 mL
90 mL
90 mL
125 mL
25 mL
25 mL
250 mL
5 L
500 mL
500 mL
1x, 100 mL
1x, 300 mL
1x, 500 mL
50 mL
5000 mL
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Croatia (6)
X
Product
Pack
Market
Pres.
Dosage
ATC
Company
20 lozenge in blister
24 pastile in blister
Y
Y
OTC
OTC
-
R02AA05
24 pastile in blister
24 pastile in blister single dose
N
N
OTC
OTC
-
R02AA05
24 pastile in blister
Y
OTC
-
R02AA05
24 pastile in blister
24 pastile in blister single dose
Y
Y
OTC
OTC
-
R02AA05
1 bočica 30 ml otopina i nastavkom za ra
Y
OTC
-
R02AA05
1 bočica nastavkom za raspršivanja sa 30
Y
OTC
-
R02AA05
Product
Pack
Reg. Nr.
Reg. Type
Reg. Date
Reg. Valid
Revocation
Company
20 lozenge in blister
24 pastile in blister
HR-H-693425328-01
HR-H-693425328-02
31-05-2016
31-05-2016
24 pastile in blister
24 pastile in blister single dose
HR-H-159234942-01
HR-H-159234942-02
29-06-2018
29-06-2018
29-06-2023
29-06-2023
24 pastile in blister
HR-H-615396087-01
19-04-2019
24 pastile in blister
24 pastile in blister single dose
HR-H-703686374-01
HR-H-703686374-02
29-06-2018
29-06-2018
29-06-2023
29-06-2023
1 bočica 30 ml otopina i nastavkom za ra
HR-H-470596257-01
31-05-2016
1 bočica nastavkom za raspršivanja sa 30
HR-H-423767127-01
19-04-2019
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Czechia (13)
X
Product
Pack
Market
Pres.
Dosage
ATC
Company
10MG/G 1X50G
Y
dental
A01AB03
2MG/ML 300ML
N
oromucosal
A01AB03
3MG/0,2MG 12
3MG/0,2MG 24
3MG/0,2MG 36
N
Y
N
oromucosal
R02AA05
3MG/0,2MG 12
3MG/0,2MG 24
N
Y
oromucosal
R02AA05
3MG/0,2MG 12
3MG/0,2MG 24
N
Y
oromucosal
R02AA05
3MG/0,2MG 12
3MG/0,2MG 24
N
Y
oromucosal
R02AA05
2MG/ML+0,5MG/ML 1X30ML
N
oromucosal
R02AA05
2MG/ML+0,5MG/ML 1X30ML
N
oromucosal
R02AA05
5MG/1MG 12X1
5MG/1MG 24X1
5MG/1MG 36X1
N
N
N
oromucosal
R02AA05
5MG/1MG 12X1
5MG/1MG 24X1
5MG/1MG 36X1
N
N
N
oromucosal
R02AA05
2MG/ML+0,5MG/ML 1X30ML
N
oromucosal
R02AA05
2MG/ML+0,5MG/ML 1X30ML
N
oromucosal
R02AA05
5MG/1MG 12X1
5MG/1MG 24X1
5MG/1MG 36X1
N
N
N
oromucosal
R02AA05
5MG/1MG 12X1
5MG/1MG 24X1
5MG/1MG 36X1
N
N
N
oromucosal
R02AA05
5MG/1,5MG 20
N
oromucosal
R02AA05
5MG/1,5MG 20
N
oromucosal
R02AA05
1,2MG/ML 100ML
1,2MG/ML 300ML
1,2MG/ML 5000ML
1,2MG/ML 500ML
1,2MG/ML 50ML
N
N
N
N
N
oromucosal
A01AB03
2MG 12
2MG 24
2MG 36
N
Y
Y
oromucosal
R02AA05
Product
Pack
Reg. Nr.
Reg. Type
Reg. Date
Reg. Valid
Revocation
Company
10MG/G 1X50G
95/ 055/11-C
NP
2MG/ML 300ML
95/ 561/97-C
NP
3MG/0,2MG 12
3MG/0,2MG 24
3MG/0,2MG 36
69/ 791/99-C
69/ 791/99-C
69/ 791/99-C
NP
NP
NP
3MG/0,2MG 12
3MG/0,2MG 24
69/ 041/07-C
69/ 041/07-C
NP
NP
3MG/0,2MG 12
3MG/0,2MG 24
69/ 040/07-C
69/ 040/07-C
NP
NP
3MG/0,2MG 12
3MG/0,2MG 24
69/ 039/07-C
69/ 039/07-C
NP
NP
2MG/ML+0,5MG/ML 1X30ML
69/ 498/13-C
NP
2MG/ML+0,5MG/ML 1X30ML
69/ 498/13-C
NP
5MG/1MG 12X1
5MG/1MG 24X1
5MG/1MG 36X1
69/ 496/13-C
69/ 496/13-C
69/ 496/13-C
NP
NP
NP
5MG/1MG 12X1
5MG/1MG 24X1
5MG/1MG 36X1
69/ 496/13-C
69/ 496/13-C
69/ 496/13-C
NP
NP
NP
2MG/ML+0,5MG/ML 1X30ML
69/ 499/13-C
NP
2MG/ML+0,5MG/ML 1X30ML
69/ 499/13-C
NP
5MG/1MG 12X1
5MG/1MG 24X1
5MG/1MG 36X1
69/ 497/13-C
69/ 497/13-C
69/ 497/13-C
NP
NP
NP
5MG/1MG 12X1
5MG/1MG 24X1
5MG/1MG 36X1
69/ 497/13-C
69/ 497/13-C
69/ 497/13-C
NP
NP
NP
5MG/1,5MG 20
69/ 722/92-C
NP
5MG/1,5MG 20
69/ 722/92-C
NP
1,2MG/ML 100ML
1,2MG/ML 300ML
1,2MG/ML 5000ML
1,2MG/ML 500ML
1,2MG/ML 50ML
95/ 008/17-C
95/ 008/17-C
95/ 008/17-C
95/ 008/17-C
95/ 008/17-C
MRP/DCP
MRP/DCP
MRP/DCP
MRP/DCP
MRP/DCP
2MG 12
2MG 24
2MG 36
69/ 836/95-C
69/ 836/95-C
69/ 836/95-C
NP
NP
NP
Product
Pack
Ex-fact
Wholesale
Net retail
Gr. retail
Company
3MG/0,2MG 12
3MG/0,2MG 24
3MG/0,2MG 36
0
0
0
3MG/0,2MG 12
3MG/0,2MG 24
0
0
5MG/1MG 12X1
5MG/1MG 24X1
5MG/1MG 36X1
0
0
0
5MG/1MG 12X1
5MG/1MG 24X1
5MG/1MG 36X1
0
0
0
5MG/1MG 12X1
5MG/1MG 24X1
5MG/1MG 36X1
0
0
0
5MG/1MG 12X1
5MG/1MG 24X1
5MG/1MG 36X1
0
0
0
1,2MG/ML 100ML
1,2MG/ML 300ML
1,2MG/ML 5000ML
1,2MG/ML 500ML
1,2MG/ML 50ML
0
0
0
0
0
2MG 12
2MG 24
2MG 36
0
0
0
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Denmark (4)
X
Product
Pack
Market
Pres.
Dosage
ATC
Company
-
-
R02AA05
Product
Pack
Reg. Nr.
Reg. Type
Reg. Date
Reg. Valid
Revocation
Company
28101063881
NP
04-06-1982
28100165654
NP
04-06-1957
28105903217
MRP
14-09-2017
28105691315
CP
28-04-2016
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Hungary (10)
X
Product
Pack
Market
Pres.
Dosage
ATC
Company
12x blister
24x blister
36x blister
N
N
N
OTC
OTC
OTC
oral
R02AA05
1x30ml glass (adagolópumpával)
N
OTC
oromucosal
R02AA05
12x blister
24x blister
36x blister
N
Y
N
OTC
OTC
OTC
oral
R02AA05
1x30ml glass (adagolópumpával)
N
OTC
oromucosal
R02AA05
24x perf single dose blister
36x perf single dose blister
N
N
OTC
OTC
-
R02AA05
12x blister
24x blister
N
Y
OTC
OTC
oral
R02AA05
12x blister
24x blister
Y
Y
OTC
OTC
oral
R02AA05
Product
Pack
Reg. Nr.
Reg. Type
Reg. Date
Reg. Valid
Revocation
Company
12x blister
24x blister
36x blister
OGYI-T-22994/04
OGYI-T-22994/05
OGYI-T-22994/06
05-03-2016
05-03-2016
05-03-2016
1x30ml glass (adagolópumpával)
OGYI-T-22994/09
18-04-2018
12x blister
24x blister
36x blister
OGYI-T-22994/01
OGYI-T-22994/02
OGYI-T-22994/03
05-03-2016
05-03-2016
05-03-2016
1x30ml glass (adagolópumpával)
OGYI-T-22994/10
18-04-2018
24x perf single dose blister
36x perf single dose blister
OGYI-T-22994/07
OGYI-T-22994/08
13-04-2018
13-04-2018
12x blister
24x blister
OGYI-T-06619/01
OGYI-T-06619/02
01-01-1998
01-01-1998
12x blister
24x blister
OGYI-T-06619/04
OGYI-T-06619/05
27-09-2006
27-09-2006
12x blister
24x blister
OGYI-T-03843/02
OGYI-T-03843/03
01-01-1992
01-01-1992
Product
Pack
Ex-fact
Wholesale
Net retail
Gr. retail
Company
12x blister
24x blister
36x blister
0
0
0
0
0
0
0
0
0
0
0
0
1x30ml glass (adagolópumpával)
0
0
0
0
12x blister
24x blister
36x blister
0
0
0
0
0
0
0
0
0
0
0
0
1x30ml glass (adagolópumpával)
0
0
0
0
24x perf single dose blister
36x perf single dose blister
0
0
0
0
0
0
0
0
12x blister
24x blister
0
0
0
0
0
0
0
0
12x blister
24x blister
0
0
0
0
0
0
0
0
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Iceland (3)
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 (15)
X
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Lithuania (0)
No result.
Malta (15)
X
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Poland (10)
X
Product
Pack
Market
Pres.
Dosage
ATC
Company
1 bottle 250 ml
1 bottle 500 ml
1 kanister 5000 ml
OTC
OTC
OTC
-
D08AC02
1 bottle 100 ml
1 bottle 300 ml
1 bottle 5 l
1 bottle 50 ml
1 bottle 500 ml
OTC
OTC
OTC
OTC
OTC
-
A01AB03
Product
Pack
Reg. Nr.
Reg. Type
Reg. Date
Reg. Valid
Revocation
Company
12 tabs
24 tabs
36 tabs
19926
19926
19926
NP
NP
NP
12 tabs
24 tabs
36 tabs
24251
24251
24251
NP
NP
NP
09-09-2022
09-09-2022
09-09-2022
1 bottle 250 ml
1 bottle 500 ml
1 kanister 5000 ml
12029/M/01
12029/M/01
12029/M/01
NP
NP
NP
1 bottle 100 ml
1 bottle 300 ml
1 bottle 5 l
1 bottle 50 ml
1 bottle 500 ml
24427
24427
24427
24427
24427
MRP
MRP
MRP
MRP
MRP
30-11-2022
30-11-2022
30-11-2022
30-11-2022
30-11-2022
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.

Romania (7)
X
Product
Pack
Market
Pres.
Dosage
ATC
Company
blister PVC/PCTFE-Al x 12 tabs de supt
blister PVC/PCTFE-Al x 24 tabs de supt
blister PVC/PCTFE-Al x 36 tabs de supt
-
-
-
OTC
OTC
OTC
-
R02AA05
blister PVC/PCTFE-Al x 12 tabs de supt
blister PVC/PCTFE-Al x 24 tabs de supt
blister PVC/PCTFE-Al x 36 tabs de supt
-
-
-
OTC
OTC
OTC
-
R02AA05
Flacon din PE tereftalat x 300 ml marc
-
OTC
-
A01AB03
2 blister transparente PVC-PVDC/Al x 12
-
OTC
-
R02AA05
2 blister transparente PVC-PVDC/Al x 12
-
OTC
-
R02AA05
2 blister transparente PVC-PVDC/Al x 12
-
OTC
-
R02AA05
2 blister PVC/Al x 10 tabs de supt
-
OTC
-
R02AA05
Product
Pack
Reg. Nr.
Reg. Type
Reg. Date
Reg. Valid
Revocation
Company
blister PVC/PCTFE-Al x 12 tabs de supt
blister PVC/PCTFE-Al x 24 tabs de supt
blister PVC/PCTFE-Al x 36 tabs de supt
-
-
-
blister PVC/PCTFE-Al x 12 tabs de supt
blister PVC/PCTFE-Al x 24 tabs de supt
blister PVC/PCTFE-Al x 36 tabs de supt
-
-
-
Flacon din PE tereftalat x 300 ml marc
-
2 blister transparente PVC-PVDC/Al x 12
-
2 blister transparente PVC-PVDC/Al x 12
-
2 blister transparente PVC-PVDC/Al x 12
-
2 blister PVC/Al x 10 tabs de supt
-
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 (6)
X
Product
Pack
Market
Pres.
Dosage
ATC
Company
stekleničko 30 ml sol zaporko in plastič
N
OTC
oral
R02AA05
steklenico 30 ml sol zaporko mehanskim p
N
OTC
oral
R02AA05
20 lozengemi (2 x 10 pastil blister)
24 lozengemi (2 x 12 pastil blister)
36 lozengemi (3 x 12 pastil blister)
N
N
N
OTC
OTC
OTC
oral
R02AA05
12 lozengemi (1 x 12 pastil blister)
24 lozengemi (2 x 12 pastil blister)
36 lozengemi (3 x 12 pastil blister)
-
N
-
OTC
OTC
OTC
oral
R02AA05
plastenka 300 ml sol navojno zaporko
N
OTC
oral
A01AB03
kapalna steklenička 10 ml sol
-
-
S01AX09
Product
Pack
Reg. Nr.
Reg. Type
Reg. Date
Reg. Valid
Revocation
Company
stekleničko 30 ml sol zaporko in plastič
5363-I-863/11
NP
12-05-2011
steklenico 30 ml sol zaporko mehanskim p
1000-4/2013-41
NP
16-07-2015
16-07-2020
20 lozengemi (2 x 10 pastil blister)
24 lozengemi (2 x 12 pastil blister)
36 lozengemi (3 x 12 pastil blister)
10023-10/2015-4
10023-10/2015-4
10023-10/2015-4
NP
NP
NP
10-06-2015
10-06-2015
10-06-2015
12 lozengemi (1 x 12 pastil blister)
24 lozengemi (2 x 12 pastil blister)
36 lozengemi (3 x 12 pastil blister)
1000-2/2013-40
1000-2/2013-40
1000-2/2013-40
NP
NP
NP
16-07-2015
16-07-2015
16-07-2015
16-07-2020
16-07-2020
16-07-2020
plastenka 300 ml sol navojno zaporko
103-110/2016-3
NP
20-12-2016
20-12-2016
20-12-2016
kapalna steklenička 10 ml sol
-
Product
Pack
Ex-fact
Wholesale
Net retail
Gr. retail
Company
stekleničko 30 ml sol zaporko in plastič
steklenico 30 ml sol zaporko mehanskim p
20 lozengemi (2 x 10 pastil blister)
24 lozengemi (2 x 12 pastil blister)
36 lozengemi (3 x 12 pastil blister)
12 lozengemi (1 x 12 pastil blister)
24 lozengemi (2 x 12 pastil blister)
36 lozengemi (3 x 12 pastil blister)
plastenka 300 ml sol navojno zaporko
kapalna steklenička 10 ml sol
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Spain (15)
X
Product
Pack
Market
Pres.
Dosage
ATC
Company
1 bottle of 100 ml
1 bottle of 250 ml
1 bottle of 50 ml
Y
Y
Y
OTC
OTC
OTC
cut
D08AC02
1 tube of 100 g
1 tube of 200 g
1 tube of 50 g
Y
Y
Y
OTC
OTC
OTC
cut
D08AC02
1 bottle of 100 ml
-
OTC
cut
D08AC02
1 bottle of 125 ml
1 bottle of 25 ml
10 frascos of 500 ml
30 frascos of 125 ml
-
Y
-
-
OTC
OTC
OTC
OTC
cut
D08AC02
1 bottle of 125 ml
1 bottle of 25 ml
10 frascos of 500 ml
30 frascos of 125 ml
Y
Y
Y
Y
OTC
OTC
OTC
OTC
cut
D08AC02
1 tube of 100 g
1 tube of 30 g
-
Y
OTC
OTC
cut
D08AC02
10 envases unidosis of 3 ml
20 envases unidosis of 3 ml
-
-
OTC
OTC
cut
D08AC02
1 bottle of 25 ml
1 bottle of 50 ml
-
-
OTC
OTC
cut
D08AC02
20 tabs
Y
OTC
USO BUCOFARÍNGEO
R02AA05
1 bottle of 30 ml
Y
OTC
cut
D08AC02
1 bottle of 500 ml
Y
OTC
cut
D08AC02
1 bottle of 40 ml
Y
OTC
cut
D08AC02
1 bottle of 60 ml
Y
OTC
cut
D08AC02
1 bottle of 30 ml
Y
OTC
cut
D08AC02
1 bottle of 25 ml
Y
OTC
cut
D08AC02
Product
Pack
Reg. Nr.
Reg. Type
Reg. Date
Reg. Valid
Revocation
Company
1 bottle of 100 ml
1 bottle of 250 ml
1 bottle of 50 ml
61846
61846
61846
01-07-1998
01-07-1998
01-07-1998
1 tube of 100 g
1 tube of 200 g
1 tube of 50 g
61513
61513
61513
01-03-1997
01-03-1997
01-03-1997
1 bottle of 100 ml
60229
01-01-1994
1 bottle of 125 ml
1 bottle of 25 ml
10 frascos of 500 ml
30 frascos of 125 ml
56549
56549
56549
56549
01-01-1986
01-01-1986
01-01-1986
01-01-1986
1 bottle of 125 ml
1 bottle of 25 ml
10 frascos of 500 ml
30 frascos of 125 ml
61109
61109
61109
61109
01-04-1996
01-04-1996
01-04-1996
01-04-1996
1 tube of 100 g
1 tube of 30 g
61110
61110
01-04-1996
01-04-1996
10 envases unidosis of 3 ml
20 envases unidosis of 3 ml
59586
59586
01-10-1992
01-10-1992
1 bottle of 25 ml
1 bottle of 50 ml
59542
59542
01-07-1992
01-07-1992
1 bottle of 30 ml
81886
17-03-2017
1 bottle of 500 ml
51606
01-10-1973
1 bottle of 40 ml
59758
01-05-1993
1 bottle of 60 ml
63873
21-05-2001
1 bottle of 30 ml
58036
01-04-1989
1 bottle of 25 ml
83917
08-03-2019
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Sweden (20)
X
Product
Pack
Reg. Nr.
Reg. Type
Reg. Date
Reg. Valid
Revocation
Company
Nationell decentral eller ömsesidig
20-09-2012
Nationell decentral eller ömsesidig
09-06-1978
Nationell decentral eller ömsesidig
09-06-1978
Nationell decentral eller ömsesidig
12-06-1992
Nationell decentral eller ömsesidig
02-05-1985
Nationell decentral eller ömsesidig
08-12-1989
Nationell decentral eller ömsesidig
24-01-2001
31-01-2020
Nationell decentral eller ömsesidig
08-12-1989
Nationell decentral eller ömsesidig
05-05-2000
Nationell decentral eller ömsesidig
02-05-1985
Nationell decentral eller ömsesidig
01-02-1961
Nationell decentral eller ömsesidig
30-06-1988
02-04-2005
Nationell decentral eller ömsesidig
08-11-1985
Nationell decentral eller ömsesidig
16-06-2016
Nationell decentral eller ömsesidig
26-06-1998
29-02-2016
Nationell decentral eller ömsesidig
13-11-2009
31-10-2013
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 (29)
X
Product
Pack
Market
Pres.
Dosage
ATC
Company
-
D
-
R02AA05
-
-
-
D
D
D
-
D08AC02
-
-
-
-
-
-
-
-
-
-
D
D
D
D
D
D
D
D
D
D
-
D08AC02
-
-
D
D
-
A01AB03
-
-
-
-
B
B
B
B
-
A01AB03
-
-
D
D
-
A01AB03
-
D
-
A01AB03
Product
Pack
Reg. Nr.
Reg. Type
Reg. Date
Reg. Valid
Revocation
Company
39901 1
Hauptzulassung
01-12-1976
27-04-2021
60340 1
60340 1
60340 1
Hauptzulassung
Hauptzulassung
Hauptzulassung
10-06-2011
10-06-2011
10-06-2011
09-06-2021
09-06-2021
09-06-2021
58026 1
Hauptzulassung
29-01-2009
28-01-2024
36030 3
Exportzulassung
19-02-1971
19-01-2021
29466 1
Hauptzulassung
11-09-1963
29-10-2023
50174 1
50174 1
50174 1
Hauptzulassung
Hauptzulassung
Hauptzulassung
26-02-1991
26-02-1991
26-02-1991
49878 1
Exportzulassung
21-07-1992
22-01-2024
53245 2
Exportzulassung
20-10-1997
22-01-2024
62150 1
Hauptzulassung
13-12-2012
12-12-2022
45174 1
Hauptzulassung
10-12-1984
29-04-2024
44490 2
44490 2
44490 2
Hauptzulassung
Hauptzulassung
Hauptzulassung
30-05-1984
30-05-1984
30-05-1984
37551 1
37551 1
37551 1
Hauptzulassung
Hauptzulassung
Hauptzulassung
02-04-1973
02-04-1973
02-04-1973
66523 1
Hauptzulassung
29-05-2017
28-05-2022
53905 2
53905 2
53905 2
53905 2
53905 2
53905 2
53905 2
53905 2
53905 2
53905 2
Hauptzulassung
Hauptzulassung
Hauptzulassung
Hauptzulassung
Hauptzulassung
Hauptzulassung
Hauptzulassung
Hauptzulassung
Hauptzulassung
Hauptzulassung
16-07-1997
16-07-1997
16-07-1997
16-07-1997
16-07-1997
16-07-1997
16-07-1997
16-07-1997
16-07-1997
16-07-1997
65894 1
Hauptzulassung
29-03-2018
28-03-2023
62923 1
Hauptzulassung
27-08-2015
62906 1
Hauptzulassung
27-08-2015
62907 1
Hauptzulassung
27-08-2015
57479 1
Hauptzulassung
07-07-2006
06-07-2021
58133 1
Hauptzulassung
11-12-2008
10-12-2023
56070 1
56070 1
Hauptzulassung
Hauptzulassung
22-03-2004
22-03-2004
21-03-2024
21-03-2024
56080 1
Hauptzulassung
22-03-2004
21-03-2024
54573 1
54573 1
54573 1
54573 1
Hauptzulassung
Hauptzulassung
Hauptzulassung
Hauptzulassung
24-12-1998
24-12-1998
24-12-1998
24-12-1998
10-03-2024
10-03-2024
10-03-2024
10-03-2024
38034 2
38034 2
Hauptzulassung
Hauptzulassung
28-08-1974
28-08-1974
38989 1
Hauptzulassung
14-04-1975
47887 1
Hauptzulassung
18-02-1987
06-07-2021
54576 1
Hauptzulassung
06-10-1998
05-10-2023
62804 2
62804 2
Hauptzulassung
Hauptzulassung
03-12-2014
03-12-2014
62804 1
62804 1
62804 1
62804 1
62804 1
62804 1
62804 1
62804 1
Hauptzulassung
Hauptzulassung
Hauptzulassung
Hauptzulassung
Hauptzulassung
Hauptzulassung
Hauptzulassung
Hauptzulassung
03-12-2014
03-12-2014
03-12-2014
03-12-2014
03-12-2014
03-12-2014
03-12-2014
03-12-2014
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.