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

clotrimazole

North America

Canada (21)
X
Product
Pack
Market
Pres.
Dosage
ATC
Company
OTC
topical/vaginal
G01AF02
OTC
topical
D01AC01
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United States (30)
X
Product
Pack
Market
Pres.
Dosage
ATC
Company
Y
Rx
topical
D01AC01
Y
Rx
topical
D01AC01
Y
Rx
topical
D01AC01
Y
Rx
topical
D01AC01
Y
OTC
vaginal
G01AF02
Y
Y
Rx
OTC
vaginal
G01AF02
Y
Rx
oral
A01AB18
N
vaginal
G01AF02
N
vaginal
G01AF02
N
vaginal
G01AF02
N
vaginal
G01AF02
N
vaginal
G01AF02
N
topical
D01AC01
N
topical
D01AC01
N
topical
D01AC01
Y
OTC
topical
D01AC01
Y
OTC
topical
D01AC01
Y
OTC
topical
D01AC01
N
oral
A01AB18
N
topical
D01AC01
Y
OTC
topical
D01AC01
N
topical
D01AC01
N
vaginal
G01AF02
N
vaginal
G01AF02
N
vaginal
G01AF02
Y
OTC
vaginal
G01AF02
Product
Pack
Reg. Nr.
Reg. Type
Reg. Date
Reg. Valid
Revocation
Company
74580/1
ANDA
29-07-1996
73306/1
ANDA
28-02-1995
78338/1
ANDA
02-09-2008
90219/1
ANDA
03-08-2010
74165/1
ANDA
16-07-1993
72641/1
72640/1
ANDA
ANDA
04-12-1995
31-08-1993
76387/1
ANDA
29-07-2004
76763/1
ANDA
28-10-2005
18052/2
NDA
30-11-1990
17717/2
NDA
30-11-1990
20574/1
NDA
24-11-1998
20525/1
NDA
29-07-1996
73249/1
ANDA
13-02-1998
17613/1
NDA
01-01-1982
17619/1
NDA
01-01-1982
18813/1
NDA
17-02-1984
18713/1
NDA
17-06-1983
18181/1
NDA
01-01-1982
18181/2
NDA
18183/1
NDA
01-01-1982
18230/2
NDA
26-12-1991
18182/2
NDA
26-12-1991
19069/1
NDA
19-04-1985
21143/1
NDA
12-04-2000
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Europe

Austria (11)
X
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Belgium (7)
X
Product
Pack
Market
Pres.
Dosage
ATC
Company
5 g
-
vaginal
D01AC01
20 g
Y
vaginal
D01AC01
1x
N
vaginal
D01AC01
Product
Pack
Reg. Nr.
Reg. Type
Reg. Date
Reg. Valid
Revocation
Company
30 g
35 g
BE112786
BE112786
-
-
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Croatia (12)
X
Product
Pack
Market
Pres.
Dosage
ATC
Company
1 tabs in blister i aplikator, 20 g krem
T
OTC
-
G01AF02
20 g kreme u tubi
Y
OTC
-
D01AC01
20 ml otopina u bočici kapaljkom
Y
OTC
-
D01AC01
20 g kreme u tubi i 3 aplikatora
Y
OTC
-
G01AF02
3 tabs in blister i 1 aplikator
T
OTC
-
G01AF02
3 tabs in blister i aplikator, 20 g krem
Y
OTC
-
G01AF02
30 ml otopina u bočici pumpicom za raspr
Y
Rx
-
D01AC01
20 g kreme u tubi
Y
Rx
-
D01AC01
3 tabs in blister
Y
Rx
-
G01AF02
20 g kreme u tubi
Y
OTC
-
D01AC01
3 vag tabs in blister
Y
OTC
-
G01AF02
1 pessary in blister i 20 g kreme u tubi
Y
OTC
-
G01AF02
Product
Pack
Reg. Nr.
Reg. Type
Reg. Date
Reg. Valid
Revocation
Company
1 tabs in blister i aplikator, 20 g krem
HR-H-388992163-01
27-12-2016
20 g kreme u tubi
HR-H-275484988-01
27-12-2016
20 ml otopina u bočici kapaljkom
HR-H-669927428-01
27-12-2016
20 g kreme u tubi i 3 aplikatora
HR-H-366109793-01
27-12-2016
3 tabs in blister i 1 aplikator
HR-H-010573123-01
27-12-2016
3 tabs in blister i aplikator, 20 g krem
HR-H-473492227-01
27-12-2016
30 ml otopina u bočici pumpicom za raspr
HR-H-992611513-01
16-11-2015
20 g kreme u tubi
HR-H-667399852-01
26-06-2017
3 tabs in blister
HR-H-718710441-01
16-11-2018
20 g kreme u tubi
HR-H-356020173-01
25-03-2016
25-03-2021
3 vag tabs in blister
HR-H-702342089-01
25-03-2016
25-03-2021
1 pessary in blister i 20 g kreme u tubi
HR-H-343372982-01
20-03-2018
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Czechia (23)
X
Product
Pack
Market
Pres.
Dosage
ATC
Company
10MG/G 1X30G
N
cut
D01AC01
100MG 6
N
vaginal
G01AF02
10MG/G 20G
10MG/G 50G
Y
N
cut
D01AC01
10MG/ML 1X40ML
Y
cut
D01AC01
200MG 3
N
vaginal
G01AF02
10MG/G 20G
Y
cut
D01AC01
0,5G 1
Y
vaginal
G01AF02
0,01G/G 35G+APL
Y
vaginal
G01AF02
500MG+10MG/G 1+20G
Y
vaginal/cut
G01AF02
10MG/ML 1X30ML
10MG/ML 1X50ML
10MG/ML 1X60ML
Y
N
N
cut
D01AC01
0,01G/ML 1X30ML
Y
cut
D01AC01
0,01G/ML 1X30ML
N
cut
D01AC01
0,01G/G 20G
0,01G/G 50G
Y
Y
cut
D01AC01
100MG 6
Y
vaginal
G01AF02
200MG 3
Y
vaginal
G01AF02
10MG/G 1X10G
10MG/G 1X20G
10MG/G 1X30G
10MG/G 1X50G
N
N
N
Y
cut
D01AC01
10MG/G 1X10G
10MG/G 1X20G
10MG/G 1X30G
10MG/G 1X50G
N
Y
N
Y
cut
D01AC01
10MG/G 1X30G
10MG/G 1X30G
Y
Y
cut
D01AC01
20MG/G 20G+APL
Y
vaginal
G01AF02
Product
Pack
Reg. Nr.
Reg. Type
Reg. Date
Reg. Valid
Revocation
Company
10MG/G 1X30G
46/ 095/91-S/C
NP
100MG 6
54/ 922/92-A/C
NP
10MG/G 20G
10MG/G 50G
26/ 953/92-S/C
26/ 953/92-S/C
NP
NP
10MG/ML 1X40ML
26/ 954/92-S/C
NP
200MG 3
54/ 922/92-B/C
NP
10MG/G 20G
26/ 202/72-C
NP
0,5G 1
54/ 200/72-A/C
NP
0,01G/G 35G+APL
54/ 605/00-C
NP
500MG+10MG/G 1+20G
54/ 033/98-C
NP
10MG/ML 1X30ML
10MG/ML 1X50ML
10MG/ML 1X60ML
26/ 944/92-S/C
26/ 944/92-S/C
26/ 944/92-S/C
NP
NP
NP
0,01G/ML 1X30ML
26/ 267/95-C
NP
0,01G/ML 1X30ML
26/ 267/95-C
NP
0,01G/G 20G
0,01G/G 50G
26/ 268/95-C
26/ 268/95-C
NP
NP
100MG 6
54/ 073/98-C
NP
200MG 3
54/ 074/98-C
NP
10MG/G 1X10G
10MG/G 1X20G
10MG/G 1X30G
10MG/G 1X50G
26/ 186/02-C
26/ 186/02-C
26/ 186/02-C
26/ 186/02-C
NP
NP
NP
NP
10MG/G 1X10G
10MG/G 1X20G
10MG/G 1X30G
10MG/G 1X50G
26/ 186/02-C
26/ 186/02-C
26/ 186/02-C
26/ 186/02-C
NP
NP
NP
NP
10MG/G 1X30G
10MG/G 1X30G
46/ 090/91-S/C/PI/001/15
46/ 090/91-S/C
PI
NP
10MG/G 1X30G
46/ 090/91-S/C
NP
20MG/G 20G+APL
54/ 848/92-C
NP
Product
Pack
Ex-fact
Wholesale
Net retail
Gr. retail
Company
10MG/G 20G
10MG/G 50G
0
0
10MG/ML 1X30ML
10MG/ML 1X50ML
10MG/ML 1X60ML
0
0
0
0,01G/G 20G
0,01G/G 50G
0
0
10MG/G 1X10G
10MG/G 1X20G
10MG/G 1X30G
10MG/G 1X50G
0
0
0
0
10MG/G 1X10G
10MG/G 1X20G
10MG/G 1X30G
10MG/G 1X50G
0
0
0
0
10MG/G 1X30G
10MG/G 1X30G
0
0
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Denmark (13)
X
Product
Pack
Reg. Nr.
Reg. Type
Reg. Date
Reg. Valid
Revocation
Company
28100913877
NP
28-02-1978
28105893316
PI
15-03-2017
28100608472
NP
15-07-1974
28105605915
PI
17-07-2015
28100608672
NP
15-07-1974
28103587803
PI
10-12-2003
28105606115
PI
17-07-2015
28101084381
NP
01-09-1982
28103536103
PI
30-09-2003
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Hungary (12)
X
Product
Pack
Market
Pres.
Dosage
ATC
Company
3x blister +1 applikátor
Y
OTC
vaginal
G01AF02
1x20g al tube
1x30g al tube
Y
Y
OTC
OTC
-
D01AC01
1x20ml plastic container
Y
OTC
topical
D01AC01
3x blister (al//al)+1 applikátor (pe/pp)
Y
OTC
vaginal
G01AF02
6x blister (al/pe)
6x blister (pa/al/pvc-al)
Y
Y
Rx
Rx
vaginal
G01AF02
3x blister (al//al)+20g tubus+1 applikát
Y
OTC
vaginal
G01AF02
1x1+20g blister és al tube
Y
OTC
vaginal
G01AF02
1x blister +20 g al tubus+pe/pp applikát
N
OTC
-
G01AF02
1x blister
Y
OTC
-
G01AF02
1x25g al tube
N
OTC
topical
D01AC01
1x20g tube
Y
OTC
topical
D01AC01
1x blister +20 g al tube
Y
OTC
vaginal
G01AF02
Product
Pack
Reg. Nr.
Reg. Type
Reg. Date
Reg. Valid
Revocation
Company
3x blister +1 applikátor
OGYI-T-09719/02
27-07-2004
1x20g al tube
1x30g al tube
OGYI-T-08110/01
OGYI-T-08110/10
25-07-2001
25-07-2001
1x20ml plastic container
OGYI-T-08110/04
25-07-2001
3x blister (al//al)+1 applikátor (pe/pp)
OGYI-T-08110/03
22-03-2006
6x blister (al/pe)
6x blister (pa/al/pvc-al)
OGYI-T-08110/06
OGYI-T-08110/05
25-07-2001
25-07-2001
3x blister (al//al)+20g tubus+1 applikát
OGYI-T-08110/02
22-03-2006
1x1+20g blister és al tube
OGYI-T-08110/07
09-09-2011
1x blister +20 g al tubus+pe/pp applikát
OGYI-T-08110/09
21-03-2012
1x blister
OGYI-T-08110/08
12-03-2012
1x25g al tube
OGYI-T-20856/01
24-04-2009
1x20g tube
OGYI-T-09719/03
27-07-2004
1x blister +20 g al tube
OGYI-T-21741/01
14-06-2011
Product
Pack
Ex-fact
Wholesale
Net retail
Gr. retail
Company
3x blister +1 applikátor
0
0
0
0
1x20g al tube
1x30g al tube
0
0
0
0
0
0
0
0
1x20ml plastic container
0
0
0
0
3x blister (al//al)+1 applikátor (pe/pp)
0
0
0
0
6x blister (al/pe)
6x blister (pa/al/pvc-al)
0
0
0
0
0
0
0
0
3x blister (al//al)+20g tubus+1 applikát
0
0
0
0
1x1+20g blister és al tube
0
0
0
0
1x blister +20 g al tubus+pe/pp applikát
0
0
0
0
1x20g tube
0
0
0
0
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Iceland (4)
X
Product
Pack
Market
Pres.
Dosage
ATC
Company
Y
OTC
-
D01AC01
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.

Ireland (19)
X
Product
Pack
Reg. Nr.
Reg. Type
Reg. Date
Reg. Valid
Revocation
Company
PPA1562/191/001
11-11-2016
PA1410/039/002
01-04-1977
PA1410/039/007
01-04-1977
PA1410/039/008
10-10-1979
PA1410/039/009
14-03-1983
PPA1463/049/001
02-09-2011
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.

Lithuania (12)
X
Product
Pack
Market
Pres.
Dosage
ATC
Company
N1 ir aplikatorius blister
OTC
vaginal
G01AF02
N6 dvisluoksnė juostelė
Rx
vaginal
G01AF02
N3 dvisluoksnė juostelė
OTC
vaginal
G01AF02
20 g N1 tube
Rx
cut
G01AF02
20 g N1 tube
Rx
cut
G01AF02
20 g N1 tube
Rx
cut
D01AC01
20 g N1 tube
Rx
cut
D01AC01
N6 blister
Rx
vaginal
G01AF02
N6 blister
N6 blister
Rx
Rx
vaginal
G01AF02
15 g N1 tube
20 g N1 tube
Rx
Rx
cut
D01AC01
15 ml N1 bottle
Rx
cut
D01AC01
Product
Pack
Reg. Nr.
Reg. Type
Reg. Date
Reg. Valid
Revocation
Company
N1 ir aplikatorius blister
LT/1/16/3993/001
DCP
10-11-2016
N6 dvisluoksnė juostelė
LT/1/93/3138/001
NP
10-06-1993
N3 dvisluoksnė juostelė
LT/1/93/3138/002
NP
26-08-1998
20 g N1 tube
LT/1/18/4274/001
NP
28-09-2018
20 g N1 tube
LT/L/18/0666/001
PI
18-06-2018
20 g N1 tube
LT/L/19/0852/001
PI
05-03-2019
20 g N1 tube
LT/1/95/1990/001
NP
05-04-1995
20 g N1 tube
LT/L/12/0075/001
PI
17-02-2012
N6 blister
LT/1/95/1990/002
NP
05-04-1995
N6 blister
N6 blister
LT/L/16/0356/001
LT/L/12/0075/002
PI
PI
18-03-2016
21-09-2012
15 g N1 tube
20 g N1 tube
LT/1/2000/2253/001
LT/1/2000/2253/002
NP
NP
08-05-2000
08-05-2000
15 ml N1 bottle
LT/1/95/1972/001
NP
15-02-1995
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Malta (28)
X
Product
Pack
Market
Pres.
Dosage
ATC
Company
OTC
-
D01AC01
OTC
-
D01AC01
OTC
-
D01AC01
Product
Pack
Reg. Nr.
Reg. Type
Reg. Date
Reg. Valid
Revocation
Company
PI908/04102A
25-04-2012
MA513/00109
09-03-2006
PI555/00602A
22-05-2013
PI1199/01001A
12-04-2019
MA639/01003
09-03-2006
PI555/00607A
27-06-2016
MA513/00101
26-05-2006
PI555/00609A
17-07-2017
MA513/00107
09-03-2006
PI555/00606A
24-07-2015
MA639/01002
08-03-2006
MA513/00110
18-12-2012
PI521/01301A
15-12-2005
MA639/01004
07-05-2015
PI555/00610A
17-07-2017
AA084/04404
05-02-2008
AA084/04403
05-02-2008
AA084/04401
26-07-2007
AA084/04402
05-02-2008
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.

Poland (15)
X
Product
Pack
Market
Pres.
Dosage
ATC
Company
1 caps
OTC
-
G01AF02
1 tabs
OTC
-
G01AF02
1 tube 20 g
1 tube 35 g
1 tube 50 g
Rp
OTC
Rp
-
G01AF02
1 tube 20 g
OTC
-
D01AC01
1 op. 15 g
1 op. 15 ml
1 op. 50 g
OTC
-
D01AC01
1 tube 15 g
1 tube 20 g
OTC
OTC
-
D01AC01
1 tube 20 g
OTC
-
D01AC01
1 tube 30 g
OTC
-
D01AC01
Product
Pack
Reg. Nr.
Reg. Type
Reg. Date
Reg. Valid
Revocation
Company
1 caps
23603
DCP
07-12-2021
1 tabs
23649
DCP
26-12-2021
1 tube 20 g
1 tube 35 g
1 tube 50 g
24123
24123
24123
DCP
DCP
DCP
18-07-2022
18-07-2022
18-07-2022
6 tabs
270/17
PI
25-08-2022
1 op. 15 g
1 op. 15 ml
1 op. 50 g
03495
03495
03495
NP
NP
NP
1 tube 15 g
1 tube 20 g
04078
04078
NP
NP
1 bottle 20 ml
23722
NP
09-02-2022
1 tube 30 g
14900
MRP
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 (12)
X
Product
Pack
Market
Pres.
Dosage
ATC
Company
1 tubee Al x 20 g cream
1 tubee Al x 30 g cream
-
-
OTC
OTC
-
D01AC01
x 1 blister PA-Al-PVC/Al x 3 vag tabs +
-
OTC
-
G01AF02
1 tubee Al x 20 g cream vaginala cu 3 ap
-
OTC
-
G01AF02
1 blister triplulaminat PVC-PVDC-PVC/Al
-
OTC
-
G01AF02
x 1 flac. din sticla bruna x 25 g sol. c
-
OTC
-
D01AC01
1 tube Al x 15 g
1 tube Al x 35 g
-
-
OTC
OTC
-
D01AC01
1 tube Al 20 g cream
1 tube Al x 35 g cream
-
-
OTC
OTC
-
D01AC01
1 tubee Al x 20 g cream
-
OTC
-
D01AC01
2 blister Al/PVC x 6 vag tabs
-
OTC
-
G01AF02
x 1 flac. PEID alb x 20 ml spray cutanat
-
OTC
-
D01AC01
1 tubee Al x 20 g cream
-
OTC
-
D01AC01
1 blister PVC/Al x 6 vag tabs
2 blister PVC/Al x 6 vag tabs
-
-
OTC
OTC
-
G01AF02
Product
Pack
Reg. Nr.
Reg. Type
Reg. Date
Reg. Valid
Revocation
Company
1 tubee Al x 20 g cream
1 tubee Al x 30 g cream
-
-
x 1 blister PA-Al-PVC/Al x 3 vag tabs +
-
1 tubee Al x 20 g cream vaginala cu 3 ap
-
1 blister triplulaminat PVC-PVDC-PVC/Al
-
x 1 flac. din sticla bruna x 25 g sol. c
-
1 tube Al x 15 g
1 tube Al x 35 g
-
-
1 tube Al 20 g cream
1 tube Al x 35 g cream
-
-
1 tubee Al x 20 g cream
-
2 blister Al/PVC x 6 vag tabs
-
x 1 flac. PEID alb x 20 ml spray cutanat
-
1 blister PVC/Al x 6 vag tabs
2 blister PVC/Al x 6 vag tabs
-
-
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Slovenia (17)
X
Product
Pack
Market
Pres.
Dosage
ATC
Company
tubo 15 g kreme
-
OTC
Dermalna uporaba
D01AC01
plastenko (z zaporko pršilnim ventilom)
-
OTC
Dermalna uporaba
D01AC01
plastenko 30 g dermalnega powd
N
OTC
Dermalna uporaba
D01AC01
tubo 20 g kreme
N
OTC
Dermalna uporaba
D01AC01
plastenko 20 ml sol
N
OTC
Dermalna uporaba
D01AC01
plastenko (z zaporko pršilnim ventilom)
N
OTC
Dermalna uporaba
D01AC01
3 vaginalnimi tabs (1 x 3 tabs blister)
-
Rx
vaginal
G01AF02
3 vaginalnimi tabs (1 x 3 tabs blister),
-
Rx
vaginal
G01AF02
1 vaginalno tab blister in 1 applicatorj
N
OTC
vaginal
G01AF02
1 vaginalno tab blister, tubo 20 g kreme
N
OTC
vaginal
G01AF02
1 vaginalno kapsulo (1 x 1 caps blister)
N
OTC
vaginal
G01AF02
tubo 20 g vaginalna kreme in 3 applicato
N
OTC
vaginal
G01AF02
3 vaginalnimi tabs (1 x 3 tabs blister)
N
OTC
vaginal
G01AF02
3 vaginalnimi tabs (1 x 3 tabs blister),
N
OTC
vaginal
G01AF02
stekleničko razpršilnikom 30 ml sol (850
-
OTC
Dermalna uporaba
D01AC01
steklenico mehanskim razpršilnikom 30 ml
N
OTC
Dermalna uporaba
D01AC01
20 ml
-
OTC
Dermalna uporaba
D01AC01
Product
Pack
Reg. Nr.
Reg. Type
Reg. Date
Reg. Valid
Revocation
Company
tubo 15 g kreme
-
plastenko (z zaporko pršilnim ventilom)
-
plastenko 30 g dermalnega powd
5363-U-I-2018/11
NP
14-06-2012
26-06-2012
26-06-2012
tubo 20 g kreme
5363-I-2016/11
NP
28-10-2011
plastenko 20 ml sol
5363-U-I-2017/11
NP
14-06-2012
26-06-2012
26-06-2012
plastenko (z zaporko pršilnim ventilom)
5363-U-I-2019/11
NP
14-06-2012
26-06-2012
26-06-2012
3 vaginalnimi tabs (1 x 3 tabs blister)
-
3 vaginalnimi tabs (1 x 3 tabs blister),
-
1 vaginalno tab blister in 1 applicatorj
103-36/2017-3
NP
08-05-2017
08-05-2017
08-05-2017
1 vaginalno tab blister, tubo 20 g kreme
103-37/2017-3
NP
24-05-2017
24-05-2017
24-05-2017
1 vaginalno kapsulo (1 x 1 caps blister)
1001-10/2017-19
NP
29-05-2019
tubo 20 g vaginalna kreme in 3 applicato
5363-I-2023/11
NP
28-10-2011
3 vaginalnimi tabs (1 x 3 tabs blister)
5363-I-2022/11
NP
28-10-2011
3 vaginalnimi tabs (1 x 3 tabs blister),
5363-I-2024/11
NP
28-10-2011
stekleničko razpršilnikom 30 ml sol (850
-
steklenico mehanskim razpršilnikom 30 ml
5363-I-2557/12
NP
13-11-2012
Product
Pack
Ex-fact
Wholesale
Net retail
Gr. retail
Company
tubo 15 g kreme
plastenko (z zaporko pršilnim ventilom)
plastenko 30 g dermalnega powd
tubo 20 g kreme
3,29
plastenko 20 ml sol
plastenko (z zaporko pršilnim ventilom)
3 vaginalnimi tabs (1 x 3 tabs blister)
3 vaginalnimi tabs (1 x 3 tabs blister),
1 vaginalno tab blister in 1 applicatorj
1 vaginalno tab blister, tubo 20 g kreme
tubo 20 g vaginalna kreme in 3 applicato
5,05
3 vaginalnimi tabs (1 x 3 tabs blister)
5,05
3 vaginalnimi tabs (1 x 3 tabs blister),
stekleničko razpršilnikom 30 ml sol (850
steklenico mehanskim razpršilnikom 30 ml
3,42
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 (16)
X
Product
Pack
Market
Pres.
Dosage
ATC
Company
1 tube of 30 g
Y
OTC
cut
D01AC01
1 bottle of 30 g
Y
Rx
cut
D01AC01
1 tube of 30 g
Y
Rx
cut
D01AC01
1 bottle of 30 ml
Y
Rx
cut
D01AC01
1 bottle of 30 g
-
Rx
cut
D01AC01
1 tube of 30 g
Y
Rx
cut
D01AC01
1 bottle of 30 ml
-
Rx
cut
D01AC01
1 tube of 20 g
Y
Rx
vaginal
G01AF02
1 tube of 30 g
-
OTC
cut
D01AC01
6 tabs
Y
OTC
vaginal
G01AF02
1 tube of 5 g
Y
OTC
vaginal
G01AF02
1 tube of 20 g
Y
OTC
vaginal
G01AF02
1 cap vaginal + 1 aplicador.
Y
OTC
vaginal
G01AF02
1 tab
Y
OTC
vaginal
G01AF02
Product
Pack
Reg. Nr.
Reg. Type
Reg. Date
Reg. Valid
Revocation
Company
1 tube of 30 g
69680
17-03-2008
1 bottle of 30 g
56826
01-09-1985
1 tube of 30 g
52626
01-04-1975
1 bottle of 30 ml
52625
01-04-1975
1 bottle of 30 g
61799
01-07-1998
1 tube of 30 g
62221
01-09-1998
1 bottle of 30 ml
61798
01-07-1998
1 tube of 20 g
62220
01-09-1998
1 tube of 30 g
55310
01-07-1981
1 tube of 5 g
59019
01-02-1993
1 tube of 20 g
56825
01-11-1985
1 cap vaginal + 1 aplicador.
78414
31-01-2014
1 tab
56755
01-10-1985
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 (12)
X
Product
Pack
Reg. Nr.
Reg. Type
Reg. Date
Reg. Valid
Revocation
Company
Nationell decentral eller ömsesidig
29-03-2012
Nationell decentral eller ömsesidig
18-04-1975
31-12-2005
Nationell decentral eller ömsesidig
29-10-2004
30-07-2009
Nationell decentral eller ömsesidig
29-08-1986
31-12-2004
Nationell decentral eller ömsesidig
25-01-1980
Nationell decentral eller ömsesidig
18-04-1975
Nationell decentral eller ömsesidig
18-04-1975
Nationell decentral eller ömsesidig
12-03-1982
28-02-2011
Nationell decentral eller ömsesidig
21-08-1996
Nationell decentral eller ömsesidig
04-02-1983
Nationell decentral eller ömsesidig
06-04-1995
Nationell decentral eller ömsesidig
09-06-1989
31-12-2011
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 (17)
X
Product
Pack
Market
Pres.
Dosage
ATC
Company
-
-
D
D
-
D01AC01
-
D
-
D01AC01
-
-
D
D
-
D01AC01
-
D
-
G01AF02
-
-
D
D
-
D01AC01
Product
Pack
Reg. Nr.
Reg. Type
Reg. Date
Reg. Valid
Revocation
Company
37510 1
37510 1
Hauptzulassung
Hauptzulassung
16-07-1973
16-07-1973
25-09-2022
25-09-2022
39725 1
Hauptzulassung
18-02-1977
25-09-2022
48679 1
48679 1
Hauptzulassung
Hauptzulassung
29-12-1989
29-12-1989
22-03-2022
22-03-2022
55962 1
Hauptzulassung
20-06-2003
19-06-2023
49767 2
49767 2
Hauptzulassung
Hauptzulassung
21-09-1990
21-09-1990
49769 2
Hauptzulassung
26-09-1990
10-05-2021
49768 1
Hauptzulassung
14-09-1990
10-05-2021
49768 2
Hauptzulassung
14-09-1990
10-05-2021
48606 1
Hauptzulassung
10-02-1988
22-08-2022
48607 1
Hauptzulassung
18-04-1990
22-08-2022
43401 1
Hauptzulassung
17-11-1980
37512 2
Hauptzulassung
17-08-1973
60954 1
Hauptzulassung
15-10-2009
37512 3
Exportzulassung
17-08-1973
37512 1
Exportzulassung
17-08-1973
45862 1
Hauptzulassung
27-12-1983
55417 1
Hauptzulassung
06-03-2001
22-08-2022
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.