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

epirubicin

North America

Canada (3)
X
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.

United States (32)
X
Product
Pack
Market
Pres.
Dosage
ATC
Company
Y
Rx
INJECTION
L01DB03
Y
Rx
INJECTION
L01DB03
Product
Pack
Reg. Nr.
Reg. Type
Reg. Date
Reg. Valid
Revocation
Company
50778/1
NDA
15-09-1999
50778/2
NDA
15-09-1999
65411/1
65408/4
ANDA
ANDA
20-08-2007
15-10-2007
91599/2
65371/2
ANDA
ANDA
12-03-2012
28-11-2007
65408/2
65411/2
ANDA
ANDA
15-10-2007
20-08-2007
91599/1
65371/1
ANDA
ANDA
12-03-2012
28-11-2007
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Europe

Austria (7)
X
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.

Belgium (18)
X
Product
Pack
Market
Pres.
Dosage
ATC
Company
10 mL
100 mL
25 mL
5 mL
50 mL
-
Y
Y
Y
-




iv/intravesical
L01DB03
10 mL
10 mL
100 mL
100 mL
25 mL
25 mL
-
-
N
-
-
N





iv/intravesical
L01DB03
10 mL
100 mL
25 mL
5 mL
N
Y
Y
Y



iv/intravesical
L01DB03
10 mL
10 mL
100 mL
25 mL
5 mL
5 mL
50 mL
Y
Y
-
-
Y
Y
-






iv/intravesical
L01DB03
100 mL
100 mL
25 mL
25 mL
5 mL
5 mL
50 mL
50 mL
N
Y
Y
N
N
N
N
N







iv/intravesical
L01DB03
10 mL
100 mL
25 mL
5 mL
75 mL
-
Y
Y
Y
Y




iv/intravesical
L01DB03
100 mL
25 mL
5 mL
50 mL
-
-
-
-



iv/intravesical
L01DB03
10 mg
N
iv/intravesical
L01DB03
50 mg
N
iv/intravesical
L01DB03
Product
Pack
Reg. Nr.
Reg. Type
Reg. Date
Reg. Valid
Revocation
Company
10 mL
100 mL
25 mL
5 mL
50 mL
BE317125
BE317152
BE317134
BE317116
BE317143
-
-
-
-
-
10 mL
10 mL
100 mL
100 mL
25 mL
25 mL
BE305636
BE305611
BE305645
BE305645
BE305627
BE305627
-
-
-
-
-
-
10 mL
100 mL
25 mL
5 mL
BE333645
BE333663
BE333654
BE333636
-
-
-
-
10 mL
10 mL
100 mL
25 mL
5 mL
5 mL
50 mL
BE321587
BE321587
BE321605
BE321596
BE321571
BE321571
BE414531
-
-
-
-
-
-
-
100 mL
100 mL
25 mL
25 mL
5 mL
5 mL
50 mL
50 mL
BE319715
BE319715
BE319697
BE319697
BE319681
BE319681
BE319706
BE319706
-
-
-
-
-
-
-
-
10 mL
100 mL
25 mL
5 mL
75 mL
BE333925
BE333952
BE333934
BE333916
BE333943
-
-
-
-
-
100 mL
25 mL
5 mL
50 mL
BE391097
BE391081
BE413147
BE413156
-
-
-
-
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Croatia (4)
X
Product
Pack
Market
Pres.
Dosage
ATC
Company
1 boca sa 100 ml otopina
1 bočica 25 ml otopina
1 bočica 5 ml otopina
1 bočica 50 ml otopina
Y
Y
Y
Y
Rx
Rx
Rx
Rx
-
L01DB03
1 bočica praškom
Y
Rx
-
L01DB03
1 bočica praškom
Y
Rx
-
L01DB03
1 bočica 25 ml otopina
1 bočica 5 ml otopina
Y
Y
Rx
Rx
-
L01DB03
Product
Pack
Reg. Nr.
Reg. Type
Reg. Date
Reg. Valid
Revocation
Company
1 boca sa 100 ml otopina
1 bočica 25 ml otopina
1 bočica 5 ml otopina
1 bočica 50 ml otopina
HR-H-247532247-04
HR-H-247532247-02
HR-H-247532247-01
HR-H-247532247-03
17-11-2017
17-11-2017
17-11-2017
17-11-2017
1 bočica praškom
HR-H-635812886-01
28-04-2015
1 bočica praškom
HR-H-692168565-01
28-04-2015
1 bočica 25 ml otopina
1 bočica 5 ml otopina
HR-H-060784644-02
HR-H-060784644-01
17-08-2018
17-08-2018
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Czechia (5)
X
Product
Pack
Market
Pres.
Dosage
ATC
Company
2MG/ML 1X100ML
2MG/ML 1X10ML
2MG/ML 1X25ML
2MG/ML 1X50ML
2MG/ML 1X5ML
N
N
Y
N
N
iv/intravesical
L01DB03
2MG/ML 1X100ML
2MG/ML 1X100ML
2MG/ML 1X10ML
2MG/ML 1X10ML
2MG/ML 1X25ML
2MG/ML 1X25ML
2MG/ML 1X50ML
2MG/ML 1X50ML
2MG/ML 1X5ML
2MG/ML 1X5ML
N
N
N
N
Y
Y
N
N
N
N
iv/intravesical
L01DB03
2MG/ML 1X100ML I
2MG/ML 1X100ML I
2MG/ML 1X100ML II
2MG/ML 1X100ML II
2MG/ML 1X10ML I
2MG/ML 1X10ML I
2MG/ML 1X10ML II
2MG/ML 1X10ML II
2MG/ML 1X25ML I
2MG/ML 1X25ML I
2MG/ML 1X25ML II
2MG/ML 1X25ML II
2MG/ML 1X50ML I
2MG/ML 1X50ML I
2MG/ML 1X50ML II
2MG/ML 1X50ML II
2MG/ML 1X5ML I
2MG/ML 1X5ML I
2MG/ML 1X5ML II
2MG/ML 1X5ML II
N
N
N
N
N
N
N
N
N
N
N
Y
N
N
N
N
N
N
N
N
iv/intravesical
L01DB03
Product
Pack
Reg. Nr.
Reg. Type
Reg. Date
Reg. Valid
Revocation
Company
2MG/ML 1X100ML
2MG/ML 1X10ML
2MG/ML 1X25ML
2MG/ML 1X50ML
2MG/ML 1X5ML
44/ 308/08-C
44/ 308/08-C
44/ 308/08-C
44/ 308/08-C
44/ 308/08-C
MRP/DCP
MRP/DCP
MRP/DCP
MRP/DCP
MRP/DCP
2MG/ML 1X100ML
2MG/ML 1X100ML
2MG/ML 1X10ML
2MG/ML 1X10ML
2MG/ML 1X25ML
2MG/ML 1X25ML
2MG/ML 1X50ML
2MG/ML 1X50ML
2MG/ML 1X5ML
2MG/ML 1X5ML
44/ 588/09-C
44/ 588/09-C
44/ 588/09-C
44/ 588/09-C
44/ 588/09-C
44/ 588/09-C
44/ 588/09-C
44/ 588/09-C
44/ 588/09-C
44/ 588/09-C
MRP/DCP
MRP/DCP
MRP/DCP
MRP/DCP
MRP/DCP
MRP/DCP
MRP/DCP
MRP/DCP
MRP/DCP
MRP/DCP
2MG/ML 1X100ML I
2MG/ML 1X100ML I
2MG/ML 1X100ML II
2MG/ML 1X100ML II
2MG/ML 1X10ML I
2MG/ML 1X10ML I
2MG/ML 1X10ML II
2MG/ML 1X10ML II
2MG/ML 1X25ML I
2MG/ML 1X25ML I
2MG/ML 1X25ML II
2MG/ML 1X25ML II
2MG/ML 1X50ML I
2MG/ML 1X50ML I
2MG/ML 1X50ML II
2MG/ML 1X50ML II
2MG/ML 1X5ML I
2MG/ML 1X5ML I
2MG/ML 1X5ML II
2MG/ML 1X5ML II
44/ 108/08-C
44/ 108/08-C
44/ 108/08-C
44/ 108/08-C
44/ 108/08-C
44/ 108/08-C
44/ 108/08-C
44/ 108/08-C
44/ 108/08-C
44/ 108/08-C
44/ 108/08-C
44/ 108/08-C
44/ 108/08-C
44/ 108/08-C
44/ 108/08-C
44/ 108/08-C
44/ 108/08-C
44/ 108/08-C
44/ 108/08-C
44/ 108/08-C
MRP/DCP
MRP/DCP
MRP/DCP
MRP/DCP
MRP/DCP
MRP/DCP
MRP/DCP
MRP/DCP
MRP/DCP
MRP/DCP
MRP/DCP
MRP/DCP
MRP/DCP
MRP/DCP
MRP/DCP
MRP/DCP
MRP/DCP
MRP/DCP
MRP/DCP
MRP/DCP
Product
Pack
Ex-fact
Wholesale
Net retail
Gr. retail
Company
2MG/ML 1X100ML
2MG/ML 1X10ML
2MG/ML 1X25ML
2MG/ML 1X50ML
2MG/ML 1X5ML
0
0
1937,01
0
0
2584,23
2MG/ML 1X100ML
2MG/ML 1X100ML
2MG/ML 1X10ML
2MG/ML 1X10ML
2MG/ML 1X25ML
2MG/ML 1X25ML
2MG/ML 1X50ML
2MG/ML 1X50ML
2MG/ML 1X5ML
2MG/ML 1X5ML
0
0
0
0
573,93
573,93
0
0
210,89
210,89
815,89
815,89
315,13
315,13
2MG/ML 1X100ML I
2MG/ML 1X100ML I
2MG/ML 1X100ML II
2MG/ML 1X100ML II
2MG/ML 1X10ML I
2MG/ML 1X10ML I
2MG/ML 1X10ML II
2MG/ML 1X10ML II
2MG/ML 1X25ML I
2MG/ML 1X25ML I
2MG/ML 1X25ML II
2MG/ML 1X25ML II
2MG/ML 1X50ML I
2MG/ML 1X50ML I
2MG/ML 1X50ML II
2MG/ML 1X50ML II
2MG/ML 1X5ML I
2MG/ML 1X5ML I
2MG/ML 1X5ML II
2MG/ML 1X5ML II
0
0
0
0
0
0
0
0
535,83
535,83
535,83
535,83
0
0
0
0
350
350
350
350
765,6
765,6
765,6
765,6
513,7
513,7
513,7
513,7
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.

Denmark (7)
X
Product
Pack
Reg. Nr.
Reg. Type
Reg. Date
Reg. Valid
Revocation
Company
28104018006
DCP
25-01-2008
28104246907
DCP
13-01-2009
28104046906
DCP
07-07-2008
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.

Hungary (4)
X
Product
Pack
Market
Pres.
Dosage
ATC
Company
1x100ml amp
1x10ml amp
1x25ml amp
1x50ml amp
1x5ml amp
N
N
Y
N
N
Rx
Rx
Rx
Rx
Rx
parenteral
L01DB03
1x25ml vial
1x50ml vial
1x5ml vial
N
N
N
Rx
Rx
Rx
parenteral
L01DB03
1x100ml vial
1x10ml vial
1x25ml vial
1x50ml vial
1x5ml vial
N
N
N
N
N
Rx
Rx
Rx
Rx
Rx
parenteral
L01DB03
1x100ml vial
1x10ml vial
1x25ml vial
1x5ml vial
1x75ml vial
N
N
N
N
N
Rx
Rx
Rx
Rx
Rx
parenteral
L01DB03
Product
Pack
Reg. Nr.
Reg. Type
Reg. Date
Reg. Valid
Revocation
Company
1x100ml amp
1x10ml amp
1x25ml amp
1x50ml amp
1x5ml amp
OGYI-T-21045/04
OGYI-T-21045/02
OGYI-T-21045/03
OGYI-T-21045/05
OGYI-T-21045/01
20-10-2009
20-10-2009
20-10-2009
20-10-2009
20-10-2009
1x25ml vial
1x50ml vial
1x5ml vial
OGYI-T-08243/02
OGYI-T-08243/03
OGYI-T-08243/01
06-12-2001
06-12-2001
06-12-2001
1x100ml vial
1x10ml vial
1x25ml vial
1x50ml vial
1x5ml vial
OGYI-T-20725/05
OGYI-T-20725/02
OGYI-T-20725/03
OGYI-T-20725/04
OGYI-T-20725/01
29-01-2009
29-01-2009
29-01-2009
29-01-2009
29-01-2009
1x100ml vial
1x10ml vial
1x25ml vial
1x5ml vial
1x75ml vial
OGYI-T-21030/05
OGYI-T-21030/02
OGYI-T-21030/03
OGYI-T-21030/01
OGYI-T-21030/04
08-10-2009
08-10-2009
08-10-2009
08-10-2009
08-10-2009
Product
Pack
Ex-fact
Wholesale
Net retail
Gr. retail
Company
1x100ml amp
1x10ml amp
1x25ml amp
1x50ml amp
1x5ml amp
0
0
6925
0
0
0
0
7229,7
0
0
0
0
8220
0
0
0
0
8631
0
0
1x25ml vial
1x50ml vial
1x5ml vial
13387
25725
2835
13976,03
26856,9
2959,74
14966
27847
3552
15714
29239
3730
1x100ml vial
1x10ml vial
1x25ml vial
1x50ml vial
1x5ml vial
0
0
0
0
0
0
0
0
0
0
0
0
0
0
0
0
0
0
0
0
1x100ml vial
1x10ml vial
1x25ml vial
1x5ml vial
1x75ml vial
29160
0
6925
1984
0
30443,04
0
7229,7
2083,2
0
31433
0
8220
2500
0
33005
0
8631
2625
0
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.

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
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.

Lithuania (6)
X
Product
Pack
Market
Pres.
Dosage
ATC
Company
10 ml N1 vial
100 ml N1 vial
25 ml N1 vial
5 ml N1 vial
50 ml N1 vial
Rx
Rx
Rx
Rx
Rx
iv/intravesical
L01DB03
10 ml N1 vial
100 ml N1 vial
25 ml N1 vial
5 ml N1 vial
50 ml N1 vial
Rx
Rx
Rx
Rx
Rx
iv/intravesical
L01DB03
100 ml, N1 vial
25 ml, N1 vial
50 ml, N1 vial
5ml, N1 vial
Rx
Rx
Rx
Rx
iv/intravesical
L01DB03
100 ml N1 bottle
25 ml N1 bottle
5 ml N1 bottle
50 ml N1 bottle
Rx
Rx
Rx
Rx
iv/intravesical
L01DB03
N1 (200 mg/100 ml) vial
N1 (50 mg/25 ml) vial
Rx
Rx
iv/intravesical
L01DB03
50 ml N1 (100mg/50 ml) vial
Rx
iv/intravesical
L01DB03
Product
Pack
Reg. Nr.
Reg. Type
Reg. Date
Reg. Valid
Revocation
Company
10 ml N1 vial
100 ml N1 vial
25 ml N1 vial
5 ml N1 vial
50 ml N1 vial
LT/1/09/1814/002
LT/1/09/1814/004
LT/1/09/1814/003
LT/1/09/1814/001
LT/1/09/1814/005
DCP
DCP
DCP
DCP
DCP
23-12-2009
23-12-2009
23-12-2009
23-12-2009
23-12-2009
10 ml N1 vial
100 ml N1 vial
25 ml N1 vial
5 ml N1 vial
50 ml N1 vial
LT/1/08/0990/002
LT/1/08/0990/005
LT/1/08/0990/003
LT/1/08/0990/001
LT/1/08/0990/004
DCP
DCP
DCP
DCP
DCP
25-01-2008
25-01-2008
25-01-2008
25-01-2008
25-01-2008
100 ml, N1 vial
25 ml, N1 vial
50 ml, N1 vial
5ml, N1 vial
LT/1/01/0931/004
LT/1/01/0931/002
LT/1/01/0931/003
LT/1/01/0931/001
NP
NP
NP
NP
29-08-2001
29-08-2001
29-08-2001
29-08-2001
100 ml N1 bottle
25 ml N1 bottle
5 ml N1 bottle
50 ml N1 bottle
LT/1/11/2421/002
LT/1/11/2421/001
LT/1/11/2421/003
LT/1/11/2421/004
RP
RP
RP
RP
21-04-2011
21-04-2011
21-04-2011
21-04-2011
N1 (200 mg/100 ml) vial
N1 (50 mg/25 ml) vial
LT/1/13/3198/002
LT/1/13/3198/001
DCP
DCP
08-02-2013
08-02-2013
50 ml N1 (100mg/50 ml) vial
LT/L/19/0935/001
PI
28-05-2019
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.

Malta (9)
X
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 (7)
X
Product
Pack
Market
Pres.
Dosage
ATC
Company
1 vial 10 ml
1 vial 100 ml
1 vial 25 ml
1 vial 5 ml
1 vial 50 ml
Rp
Rp
Rp
Rp
Rp
-
L01DB03
1 vial 10 ml
1 vial 100 ml
1 vial 25 ml
1 vial 5 ml
1 vial 50 ml
Lz
Lz
Lz
Lz
Lz
-
L01DB03
1 vial 100 ml
1 vial 25 ml
1 vial 5 ml
1 vial 50 ml
Lz
Lz
Lz
Lz
-
L01DB03
1 vial 100 ml
1 vial 25 ml
1 vial 5 ml
1 vial 50 ml
Lz
Lz
Lz
Lz
-
L01DB03
1 vial 10 ml
1 vial 100 ml
1 vial 25 ml
1 vial 5 ml
1 vial 50 ml
Rp
Rp
Rp
Rp
Rp
-
L01DB03
1 vial 100 ml
1 vial 25 ml
1 vial 25 ml
1 vial 5 ml
Lz
Lz
Lz
Lz
-
L01DB03
1 vial 5 ml
1 vial 5 ml
Lz
Lz
-
L01DB03
Product
Pack
Reg. Nr.
Reg. Type
Reg. Date
Reg. Valid
Revocation
Company
1 vial 10 ml
1 vial 100 ml
1 vial 25 ml
1 vial 5 ml
1 vial 50 ml
14827
14827
14827
14827
14827
DCP
DCP
DCP
DCP
DCP
1 vial 10 ml
1 vial 100 ml
1 vial 25 ml
1 vial 5 ml
1 vial 50 ml
17072
17072
17072
17072
17072
DCP
DCP
DCP
DCP
DCP
1 vial 100 ml
1 vial 25 ml
1 vial 5 ml
1 vial 50 ml
16728
16728
16728
16728
NP
NP
NP
NP
11-12-2018
11-12-2018
11-12-2018
11-12-2018
1 vial 100 ml
1 vial 25 ml
1 vial 5 ml
1 vial 50 ml
11043
11043
11043
11043
NP
NP
NP
NP
1 vial 10 ml
1 vial 100 ml
1 vial 25 ml
1 vial 5 ml
1 vial 50 ml
14603
14603
14603
14603
14603
DCP
DCP
DCP
DCP
DCP
11-02-2019
11-02-2019
11-02-2019
11-02-2019
11-02-2019
1 vial 100 ml
1 vial 25 ml
1 vial 25 ml
1 vial 5 ml
07525
07525
07525
07525
NP
NP
NP
NP
1 vial 5 ml
1 vial 5 ml
07524
07524
NP
NP
12-02-2018
12-02-2018
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 (3)
X
Product
Pack
Market
Pres.
Dosage
ATC
Company
x 1 flac. a 100ml sol. inj. x 200mg (20
x 1 flac. a 10 ml sol. inj. x 20mg (20mg
x 1 flac. a 25 ml sol. inj. x 50mg (50mg
x 1 flac. a 5 ml sol. inj. x 10mg (10mg/
x 1 flac. a 50 ml sol. inj. x 100mg (100
-
-
-
-
-
PR
PR
PR
PR
PR
-
L01DB03
1 flac. din sticla incolora, avand capac
-
PR
-
L01DB03
1 flac. din sticla incolora, avand capac
-
PR
-
L01DB03
Product
Pack
Reg. Nr.
Reg. Type
Reg. Date
Reg. Valid
Revocation
Company
x 1 flac. a 100ml sol. inj. x 200mg (20
x 1 flac. a 10 ml sol. inj. x 20mg (20mg
x 1 flac. a 25 ml sol. inj. x 50mg (50mg
x 1 flac. a 5 ml sol. inj. x 10mg (10mg/
x 1 flac. a 50 ml sol. inj. x 100mg (100
-
-
-
-
-
1 flac. din sticla incolora, avand capac
-
1 flac. din sticla incolora, avand capac
-
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Slovenia (8)
X
Product
Pack
Market
Pres.
Dosage
ATC
Company
1 vial 10 ml sol
1 vial 100 ml sol
1 vial 25 ml sol
1 vial 5 ml sol
1 vial 50 ml sol
-
-
-
-
-
Rx
Rx
Rx
Rx
Rx
iv
L01DB03
1 vial 100 ml conc
1 vial 25 ml conc
1 vial 5 ml conc
1 vial 50 ml conc
T
T
T
T
Rx
Rx
Rx
Rx
iv
L01DB03
1 vial 100 ml sol
1 vial 25 ml sol
1 vial 5 ml sol
1 vial 50 ml sol
-
-
-
-
Rx
Rx
Rx
Rx
iv
L01DB03
1 vial 25 ml sol
1 vial 5 ml sol
N
N
Rx
Rx
iv/intravesical
L01DB03
1 vial 100 ml sol
1 vial 25 ml sol
N
N
Rx
Rx
iv
L01DB03
1 vial 10 ml sol
1 vial 100 ml sol
1 vial 25 ml sol
1 vial 5 ml sol
1 vial 75 ml sol
-
N
N
N
-
Rx
Rx
Rx
Rx
Rx
iv
L01DB03
1 vial 25 ml sol
1 vial 5 ml sol
N
N
Rx
Rx
iv/intravesical
L01DB03
steklenička 10mg lyophila in ampula 5ml
steklenička 50mg lyophila
-
-
Rx
Rx
parenteral
L01DB03
Product
Pack
Reg. Nr.
Reg. Type
Reg. Date
Reg. Valid
Revocation
Company
1 vial 10 ml sol
1 vial 100 ml sol
1 vial 25 ml sol
1 vial 5 ml sol
1 vial 50 ml sol
-
-
-
-
-
1 vial 100 ml conc
1 vial 25 ml conc
1 vial 5 ml conc
1 vial 50 ml conc
5363-I-184/10
5363-I-182/10
5363-I-181/10
5363-I-183/10
NP
NP
NP
NP
19-01-2010
19-01-2010
19-01-2010
19-01-2010
1 vial 100 ml sol
1 vial 25 ml sol
1 vial 5 ml sol
1 vial 50 ml sol
103-151/2014-2
103-151/2014-2
103-151/2014-2
103-151/2014-2
MRP
MRP
MRP
MRP
03-11-2014
03-11-2014
03-11-2014
03-11-2014
03-11-2014
03-11-2014
03-11-2014
03-11-2014
03-01-2015
03-01-2015
03-01-2015
03-01-2015
1 vial 25 ml sol
1 vial 5 ml sol
103-96/2019-3
103-96/2019-3
DCP
DCP
14-02-2020
14-02-2020
1 vial 100 ml sol
1 vial 25 ml sol
103-38/2016-3
103-38/2016-3
DCP
DCP
25-08-2016
25-08-2016
25-08-2016
25-08-2016
25-08-2016
25-08-2016
1 vial 10 ml sol
1 vial 100 ml sol
1 vial 25 ml sol
1 vial 5 ml sol
1 vial 75 ml sol
10121-252/2019-5
10121-252/2019-5
10121-252/2019-5
10121-252/2019-5
10121-252/2019-5
DCP
DCP
DCP
DCP
DCP
12-08-2019
12-08-2019
12-08-2019
12-08-2019
12-08-2019
1 vial 25 ml sol
1 vial 5 ml sol
103-109/2015-3
103-109/2015-3
NP
NP
02-11-2015
02-11-2015
02-11-2015
02-11-2015
02-05-2017
02-05-2017
steklenička 10mg lyophila in ampula 5ml
steklenička 50mg lyophila
-
-
Product
Pack
Ex-fact
Wholesale
Net retail
Gr. retail
Company
1 vial 10 ml sol
1 vial 100 ml sol
1 vial 25 ml sol
1 vial 5 ml sol
1 vial 50 ml sol
1 vial 100 ml conc
1 vial 25 ml conc
1 vial 5 ml conc
1 vial 50 ml conc
1 vial 100 ml sol
1 vial 25 ml sol
1 vial 5 ml sol
1 vial 50 ml sol
1 vial 25 ml sol
1 vial 5 ml sol
87,82
19,98
1 vial 10 ml sol
1 vial 100 ml sol
1 vial 25 ml sol
1 vial 5 ml sol
1 vial 75 ml sol
315,61
87,82
19,98
1 vial 25 ml sol
1 vial 5 ml sol
steklenička 10mg lyophila in ampula 5ml
steklenička 50mg lyophila
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 (9)
X
Product
Pack
Market
Pres.
Dosage
ATC
Company
1 vial of 100 ml
1 vial of 25 ml
1 vial of 5 ml
1 vial of 50 ml
-
-
-
-
Rx
Rx
Rx
Rx
iv/intravesical
L01DB03
1 vial of 10 ml
1 vial of 100 ml
1 vial of 25 ml
1 vial of 5 ml
1 vial of 50 ml
-
Y
Y
Y
-
Rx
Rx
Rx
Rx
Rx
iv/intravesical
L01DB03
1 vial of 100 ml
1 vial of 25 ml
1 vial of 5 ml
-
Y
-
Rx
Rx
Rx
iv/intravesical
L01DB03
1 vial of 100 ml
1 vial of 25 ml
1 vial of 5 ml
1 vial of 50 ml
-
-
-
-
Rx
Rx
Rx
Rx
VÍA INTRAVESICAL, VÍA INTRAVENOSA
L01DB03
1 vial of 100 ml
1 vial of 25 ml
1 vial of 5 ml
1 vial of 50 ml
-
-
-
-
Rx
Rx
Rx
Rx
iv/intravesical
L01DB03
1 vial of 100 ml
1 vial of 25 ml
1 vial of 5 ml
1 vial of 75 ml
Y
Y
-
-
Rx
Rx
Rx
Rx
iv/intravesical
L01DB03
1 vial + 1 amp of solv
50 vials + 50 amp of solv
Y
Y
Rx
Rx
iv/intravesical
L01DB03
1 vial of 100 ml
1 vial of 25 ml
1 vial of 5 ml
25 vials of 25 ml
50 vials of 5 ml
Y
Y
Y
Y
Y
Rx
Rx
Rx
Rx
Rx
VÍA INTRAVESICAL, VÍA INTRAVENOSA
L01DB03
1 vial + 1 amp of solv
25 vials + 25 amp of solv
Y
Y
Rx
Rx
iv/intravesical
L01DB03
Product
Pack
Reg. Nr.
Reg. Type
Reg. Date
Reg. Valid
Revocation
Company
1 vial of 100 ml
1 vial of 25 ml
1 vial of 5 ml
1 vial of 50 ml
71347
71347
71347
71347
01-12-2010
01-12-2010
01-12-2010
01-12-2010
1 vial of 10 ml
1 vial of 100 ml
1 vial of 25 ml
1 vial of 5 ml
1 vial of 50 ml
71700
71700
71700
71700
71700
01-02-2010
01-02-2010
01-02-2010
01-02-2010
01-02-2010
1 vial of 100 ml
1 vial of 25 ml
1 vial of 5 ml
70523
70523
70523
16-12-2009
16-12-2009
16-12-2009
1 vial of 100 ml
1 vial of 25 ml
1 vial of 5 ml
1 vial of 50 ml
67794
67794
67794
67794
08-05-2006
08-05-2006
08-05-2006
08-05-2006
1 vial of 100 ml
1 vial of 25 ml
1 vial of 5 ml
1 vial of 50 ml
69868
69868
69868
69868
09-06-2008
09-06-2008
09-06-2008
09-06-2008
1 vial of 100 ml
1 vial of 25 ml
1 vial of 5 ml
1 vial of 75 ml
70763
70763
70763
70763
05-04-2010
05-04-2010
05-04-2010
05-04-2010
1 vial + 1 amp of solv
50 vials + 50 amp of solv
57200
57200
01-12-1986
01-12-1986
1 vial of 100 ml
1 vial of 25 ml
1 vial of 5 ml
25 vials of 25 ml
50 vials of 5 ml
60847
60847
60847
60847
60847
01-12-1995
01-12-1995
01-12-1995
01-12-1995
01-12-1995
1 vial + 1 amp of solv
25 vials + 25 amp of solv
57201
57201
01-10-1986
01-10-1986
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Sweden (12)
X
Product
Pack
Reg. Nr.
Reg. Type
Reg. Date
Reg. Valid
Revocation
Company
Nationell decentral eller ömsesidig
29-10-2010
Nationell decentral eller ömsesidig
10-01-2003
Nationell decentral eller ömsesidig
28-08-2009
28-08-2012
Nationell decentral eller ömsesidig
30-01-2009
31-10-2010
Nationell decentral eller ömsesidig
06-10-2006
05-07-2017
Nationell decentral eller ömsesidig
24-11-2011
30-06-2016
Nationell decentral eller ömsesidig
12-12-2008
30-11-2011
Nationell decentral eller ömsesidig
19-06-2008
Nationell decentral eller ömsesidig
21-08-2009
Nationell decentral eller ömsesidig
11-12-1987
30-06-2014
Nationell decentral eller ömsesidig
08-12-1989
31-05-2016
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Switzerland (23)
X
Product
Pack
Market
Pres.
Dosage
ATC
Company
Product
Pack
Reg. Nr.
Reg. Type
Reg. Date
Reg. Valid
Revocation
Company
56243 3
Hauptzulassung
04-06-2003
03-06-2023
56243 1
Hauptzulassung
04-06-2003
03-06-2023
56243 2
Hauptzulassung
04-06-2003
03-06-2023
58676 1
Exportzulassung
14-11-2008
13-11-2023
58676 5
Exportzulassung
14-11-2008
13-11-2023
58676 4
Exportzulassung
14-11-2008
13-11-2023
58676 3
Exportzulassung
14-11-2008
13-11-2023
58676 2
Exportzulassung
14-11-2008
13-11-2023
50359 1
Hauptzulassung
25-06-1990
20-09-2024
50359 3
Hauptzulassung
25-06-1990
20-09-2024
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