All the information on this site is from our Global Pharmaceutical Database.
G01AF04
A07AC01
J02AB01
D01AC02
S02AA13
miconazole
For informational purposes only, X-Pharma does not provide medical advice.
SPC/PIL of the products can differ from this general indication.
A01AB09SPC/PIL of the products can differ from this general indication.
G01AF04
A07AC01
J02AB01
D01AC02
S02AA13
North America
Canada (17)
X
United States (34)Product
Pack
Market
Pres.
Dosage
ATC
Company
OTC
topical/vaginal
G01AF04
OTC
topical/vaginal
G01AF04
OTC
topical/vaginal
G01AF04
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 (3)
X
Belgium (10)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 (6)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 (0)Product
Pack
Market
Pres.
Dosage
ATC
Company
Product
Pack
Reg. Nr.
Reg. Type
Reg. Date
Reg. Valid
Revocation
Company
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No result.
Denmark (6)
X
Hungary (0)Product
Pack
Market
Pres.
Dosage
ATC
Company
Product
Pack
Reg. Nr.
Reg. Type
Reg. Date
Reg. Valid
Revocation
Company
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No result.
Iceland (0)
No result.
Ireland (6)
X
Lithuania (7)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 (15)Product
Pack
Market
Pres.
Dosage
ATC
Company
30 g ir matavimo šaukštas (5 ml) N1 tube
40 g ir matavimo šaukštas (5 ml) N1 tube
40 g ir matavimo šaukštas (5 ml) N1 tube
Rx
Rx
Rx
vartoti per burną;vartoti ant burnos gleivinės
A01AB09
40 g ir matavimo šaukštas N1 tube
40 g N1 tube
40 g N1 tube
Rx
Rx
Rx
oromucosal/oral
A01AB09
40 g ir matavimo šaukštas (5 ml), N1 tub
40 g N1 + matavimo šaukštas tube
40 g N1 + matavimo šaukštas tube
Rx
Rx
Rx
oral
A01AB09
Product
Pack
Reg. Nr.
Reg. Type
Reg. Date
Reg. Valid
Revocation
Company
40 g N1 + matavimo šaukštas tube
LT/L/18/0698/001
PI
05-07-2018
30 g ir matavimo šaukštas (5 ml) N1 tube
40 g ir matavimo šaukštas (5 ml) N1 tube
40 g ir matavimo šaukštas (5 ml) N1 tube
LT/1/97/2125/001
LT/1/97/2125/002
LT/1/97/2125/002
NP
NP
NP
02-07-1997
02-07-1997
02-07-1997
40 g ir matavimo šaukštas N1 tube
40 g N1 tube
40 g N1 tube
LT/L/18/0611/001
LT/L/11/0049/001
LT/L/11/0049/001
PI
PI
PI
12-03-2018
22-07-2011
22-07-2011
40 g ir 5 ml graduotas matavimo šaukštas
LT/L/15/0271/001
PI
27-05-2015
40 g ir matavimo šaukštas (5 ml), N1 tub
40 g N1 + matavimo šaukštas tube
40 g N1 + matavimo šaukštas tube
LT/L/15/0304/001
LT/L/18/0647/001
LT/L/18/0647/001
PI
PI
PI
19-10-2015
25-05-2018
25-05-2018
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X
Poland (19)Product
Pack
Market
Pres.
Dosage
ATC
Company
Product
Pack
Reg. Nr.
Reg. Type
Reg. Date
Reg. Valid
Revocation
Company
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X
Romania (3)Product
Pack
Market
Pres.
Dosage
ATC
Company
Product
Pack
Reg. Nr.
Reg. Type
Reg. Date
Reg. Valid
Revocation
Company
1 op. 20 g
1 op. 30 g
1 op. 30 g
204/10
441/12
441/12
PI
PI
PI
15-11-2020
30-07-2017
30-07-2017
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X
Slovenia (6)Product
Pack
Market
Pres.
Dosage
ATC
Company
Product
Pack
Reg. Nr.
Reg. Type
Reg. Date
Reg. Valid
Revocation
Company
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X
Spain (5)Product
Pack
Market
Pres.
Dosage
ATC
Company
7 vaginalnimi globulami dvojnem traku
N
Rx
vaginal
G01AF04
plastenka 14 tabs
-
Rx
gingival
A01AB09
Product
Pack
Reg. Nr.
Reg. Type
Reg. Date
Reg. Valid
Revocation
Company
7 vaginalnimi globulami dvojnem traku
5363-I-133/12
NP
20-01-2012
plastenka 14 tabs
5363-U-I-1964/12
MRP
02-09-2014
23-09-2014
23-09-2014
Product
Pack
Ex-fact
Wholesale
Net retail
Gr. retail
Company
steklenička 30 ml (20mg/1ml)
5 ampul 20 ml (200mg/20ml)
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X
Sweden (4)Product
Pack
Market
Pres.
Dosage
ATC
Company
1 bottle of 125 ml
1 bottle of 50 ml
1 bottle of 50 ml
Y
-
-
Rx
Rx
Rx
cut
D01AC02
Product
Pack
Reg. Nr.
Reg. Type
Reg. Date
Reg. Valid
Revocation
Company
1 bottle of 125 ml
1 bottle of 50 ml
1 bottle of 50 ml
52875
52875
52875
01-05-1975
01-05-1975
01-05-1975
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X
Switzerland (4)Product
Pack
Market
Pres.
Dosage
ATC
Company
Product
Pack
Reg. Nr.
Reg. Type
Reg. Date
Reg. Valid
Revocation
Company
Nationell decentral eller ömsesidig
11-04-2008
01-07-2013
Nationell decentral eller ömsesidig
30-09-2005
30-04-2009
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X
Product
Pack
Market
Pres.
Dosage
ATC
Company
Product
Pack
Reg. Nr.
Reg. Type
Reg. Date
Reg. Valid
Revocation
Company
57686 2
57686 2
57686 2
Hauptzulassung
Hauptzulassung
Hauptzulassung
13-05-2008
13-05-2008
13-05-2008
12-05-2023
12-05-2023
12-05-2023
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