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

amphotericin B

North America

Canada (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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United States (13)
X
Product
Pack
Market
Pres.
Dosage
ATC
Company
N
INJECTION
J02AA01
N
INJECTION
J02AA01
Y
Rx
INJECTION
J02AA01
N
topical
G01AA03
N
topical
G01AA03
N
topical
G01AA03
N
INJECTION
J02AA01
Product
Pack
Reg. Nr.
Reg. Type
Reg. Date
Reg. Valid
Revocation
Company
64141/1
ANDA
23-12-1996
62728/1
ANDA
13-04-1987
64062/1
ANDA
31-03-1995
63206/1
ANDA
29-04-1992
60570/1
ANDA
01-01-1982
50313/1
NDA
01-01-1982
50314/1
NDA
01-01-1982
60517/1
ANDA
01-01-1982
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Europe

Austria (7)
X
Product
Pack
Reg. Nr.
Reg. Type
Reg. Date
Reg. Valid
Revocation
Company
15121
23-08-1972
1-25353
16-04-2004
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Belgium (2)
X
Product
Pack
Market
Pres.
Dosage
ATC
Company
20 mL
20 mL
Y
-

iv
J02AA01
Product
Pack
Reg. Nr.
Reg. Type
Reg. Date
Reg. Valid
Revocation
Company
20 mL
20 mL
BE199263
BE199263
-
-
Product
Pack
Ex-fact
Wholesale
Net retail
Gr. retail
Company
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Croatia (1)
X
Product
Pack
Market
Pres.
Dosage
ATC
Company
1 bočica 20 ml conc i jednokratna igla
10 bočica 20 ml conc i 10 jednokratnih i
Y
Y
Rx
Rx
-
J02AA01
Product
Pack
Reg. Nr.
Reg. Type
Reg. Date
Reg. Valid
Revocation
Company
1 bočica 20 ml conc i jednokratna igla
10 bočica 20 ml conc i 10 jednokratnih i
HR-H-747381908-01
HR-H-747381908-02
31-05-2019
31-05-2019
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Czechia (1)
X
Product
Pack
Market
Pres.
Dosage
ATC
Company
5MG/ML 10X10ML
5MG/ML 10X20ML
N
Y
iv
J02AA01
Product
Pack
Reg. Nr.
Reg. Type
Reg. Date
Reg. Valid
Revocation
Company
5MG/ML 10X10ML
5MG/ML 10X20ML
15/ 560/99-C
15/ 560/99-C
NP
NP
Product
Pack
Ex-fact
Wholesale
Net retail
Gr. retail
Company
5MG/ML 10X10ML
5MG/ML 10X20ML
0
25583,15
29648,09
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Denmark (6)
X
Product
Pack
Reg. Nr.
Reg. Type
Reg. Date
Reg. Valid
Revocation
Company
28104531209
PI
04-08-2009
28104879211
PI
05-07-2011
28103220901
PI
13-02-2001
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Hungary (2)
X
Product
Pack
Market
Pres.
Dosage
ATC
Company
10x20ml vial
N
Rx
parenteral
J02AA01
10x1darab vial + 10x1 db buborékcsomagol
N
Rx
parenteral
J02AA01
Product
Pack
Reg. Nr.
Reg. Type
Reg. Date
Reg. Valid
Revocation
Company
10x20ml vial
OGYI-T-06918/01
01-01-1999
10x1darab vial + 10x1 db buborékcsomagol
OGYI-T-05717/01
01-01-1997
Product
Pack
Ex-fact
Wholesale
Net retail
Gr. retail
Company
10x20ml vial
391768
409005,79
409996
430496
10x1darab vial + 10x1 db buborékcsomagol
538709
562412,2
563402
591572
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Iceland (1)
X
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
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 (2)
X
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.

Lithuania (0)
No result.
Malta (2)
X
Product
Pack
Reg. Nr.
Reg. Type
Reg. Date
Reg. Valid
Revocation
Company
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Poland (4)
X
Product
Pack
Market
Pres.
Dosage
ATC
Company
10 vial 10 ml
10 vial 20 ml
2 vial 20 ml + 2 needles with filtrem
Lz
Lz
Lz
-
J02AA01
1 vial 50 mg + filtr membrane
10 vial 50 mg + filtr membrane
Rp
Rp
-
J02AA01
Product
Pack
Reg. Nr.
Reg. Type
Reg. Date
Reg. Valid
Revocation
Company
10 vial 10 ml
10 vial 20 ml
2 vial 20 ml + 2 needles with filtrem
09739
09739
09739
NP
NP
NP
1 vial 50 mg + filtr membrane
10 vial 50 mg + filtr membrane
08000
08000
NP
NP
1 vial 50 mg
139/19
PI
05-04-2024
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Romania (0)
No result.
Slovenia (14)
X
Product
Pack
Market
Pres.
Dosage
ATC
Company
1 vial praškom
-
Rx
parenteral
J02AA01
10 vial (15 ml) powd in 10 filtri
10 vial (20 ml) powd in 10 filtri
10 vial (30 ml) powd in 10 filtri
N
N
-
Rx
Rx
Rx
iv
J02AA01
steklenička 50 ml suspenzije
-
Rx
parenteral
J02AA01
20 tabs
-
Rx
parenteral
J02AA01
1 vial praškom
N
Rx
iv
J02AA01
1 vial praškom
N
Rx
iv
J02AA01
1 vial 10 ml
-
Rx
parenteral
J02AA01
1 vial 50 mg powd
-
parenteral
J02AA01
1 stekleničko iz rjavega stekla 40 ml su
-
-
J02AA01
1 stekleničko 40 ml suspenzije
-
-
J02AA01
1 stekleničko 40ml suspenzije
-
-
J02AA01
Product
Pack
Reg. Nr.
Reg. Type
Reg. Date
Reg. Valid
Revocation
Company
1 vial praškom
-
10 vial (15 ml) powd in 10 filtri
10 vial (20 ml) powd in 10 filtri
10 vial (30 ml) powd in 10 filtri
10021-162/2019-5
10021-162/2019-5
10021-162/2019-5
NP
NP
NP
15-04-2020
15-04-2020
15-04-2020
steklenička 50 ml suspenzije
-
1 vial praškom
5363-U-I-11/08
NP
20-08-2013
12-04-2011
12-10-2013
1 vial praškom
5363-U-I-10/08
NP
20-08-2013
12-04-2011
12-10-2013
1 stekleničko iz rjavega stekla 40 ml su
4261-609/2012
-
16-11-2012
16-11-2013
1 stekleničko 40 ml suspenzije
841-112/2018
-
26-09-2018
26-09-2019
1 stekleničko 40ml suspenzije
/
-
17-09-2014
17-09-2015
1 vial praškom
842-27/2019
-
22-02-2019
22-02-2020
1 vial praškom
842-52/2018
-
19-02-2018
19-02-2019
Product
Pack
Ex-fact
Wholesale
Net retail
Gr. retail
Company
10 vial (15 ml) powd in 10 filtri
10 vial (20 ml) powd in 10 filtri
10 vial (30 ml) powd in 10 filtri
1567,55
steklenička 50 ml suspenzije
1 stekleničko iz rjavega stekla 40 ml su
1 stekleničko 40 ml suspenzije
1 stekleničko 40ml suspenzije
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Spain (4)
X
Product
Pack
Reg. Nr.
Reg. Type
Reg. Date
Reg. Valid
Revocation
Company
1 vial
10 vials
62517
62517
01-08-1999
01-08-1999
1 vial
10 vials
62516
62516
01-08-1999
01-08-1999
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Sweden (8)
X
Product
Pack
Reg. Nr.
Reg. Type
Reg. Date
Reg. Valid
Revocation
Company
Nationell decentral eller ömsesidig
24-05-1996
31-03-2013
Nationell decentral eller ömsesidig
10-01-1992
PI
PI
PI
05-10-2011
23-03-2016
25-07-2012
31-10-2016
31-01-2018
31-01-2018
PI
PI
PI
18-06-2014
07-09-2011
12-12-2018
31-12-2015
31-12-2015
Nationell decentral eller ömsesidig
20-03-1996
01-09-2012
Nationell decentral eller ömsesidig
16-06-1972
28-02-2010
Nationell decentral eller ömsesidig
24-11-1959
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 (5)
X
Product
Pack
Reg. Nr.
Reg. Type
Reg. Date
Reg. Valid
Revocation
Company
53342 1
53342 1
Hauptzulassung
Hauptzulassung
19-12-1996
19-12-1996
37244 1
Hauptzulassung
01-07-1974
16-06-2024
37897 2
Hauptzulassung
19-06-1974
16-06-2024
37245 1
Hauptzulassung
07-05-1974
16-06-2024
31096 1
Hauptzulassung
05-11-1964
13-10-2024
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