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

glyceryl trinitrate

North America

Canada (25)
X
Product
Pack
Market
Pres.
Dosage
ATC
Company
Ethical
transdermal
C01DA02
Ethical
transdermal
C01DA02
Ethical
transdermal
C01DA02
Ethical
transdermal
C01DA02
Ethical
transdermal
C01DA02
Ethical
transdermal
C01DA02
Ethical
transdermal
C01DA02
Ethical
transdermal
C01DA02
Ethical
transdermal
C01DA02
Ethical
transdermal
C01DA02
Ethical
transdermal
C01DA02
Ethical
sublingual
C01DA02
Ethical
sublingual
C01DA02
Ethical
sublingual
C01DA02
Ethical
transdermal
C01DA02
Ethical
transdermal
C01DA02
Ethical
transdermal
C01DA02
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 (70)
X
Product
Pack
Market
Pres.
Dosage
ATC
Company
Y
Rx
sublingual
C01DA02
N
INJECTION
C01DA02
N
INJECTION
C01DA02
Y
Rx
transdermal
C01DA02
Y
Rx
transdermal
C01DA02
Y
Rx
transdermal
C01DA02
Y
Rx
transdermal
C01DA02
Y
Rx
transdermal
C01DA02
Y
Rx
transdermal
C01DA02
N
INJECTION
C01DA02
Y
N
N
Rx

transdermal
C01DA02
N
transdermal
C01DA02
N
N
Y


Rx
transdermal
C01DA02
Y
transdermal
C01DA02
N
sublingual
C01DA02
Y
Rx
sublingual
C01DA02
Y
Rx
sublingual
C01DA02
N
sublingual
C01DA02
Y
Rx
sublingual
C01DA02
Y
Rx
sublingual
C01DA02
N
transdermal
C01DA02
N
N
Y


Rx
transdermal
C01DA02
Y
transdermal
C01DA02
N
sublingual
C01DA02
Y
Rx
sublingual
C01DA02
Y
Rx
sublingual
C01DA02
N
Y

Rx
transdermal
C01DA02
Y
transdermal
C01DA02
N
Injection
C01DA02
Y
Rx
transdermal
C01DA02
N
N

INJECTION
C01DA02
Y
Rx
INJECTION
C01DA02
N
INJECTION
C01DA02
N
Injection
C01DA02
N
INJECTION
C01DA02
N
INJECTION
C01DA02
Y
Rx
sublingual
C01DA02
Y
Rx
sublingual
C01DA02
Y
Rx
sublingual
C01DA02
N
INJECTION
C01DA02
N
N

INJECTION
C01DA02
N
N

INJECTION
C01DA02
Y
Rx
intra-anal
C05AE01
N
N
N
N
N




transdermal
C01DA02
N
INJECTION
C01DA02
N
INJECTION
C01DA02
Product
Pack
Reg. Nr.
Reg. Type
Reg. Date
Reg. Valid
Revocation
Company
208424/1
NDA
08-06-2016
89771/1
ANDA
30-08-1996
89772/1
ANDA
30-08-1996
89774/1
ANDA
30-08-1996
18672/2
NDA
30-08-1983
71159/1
ANDA
28-02-1990
18621/1
NDA
05-01-1982
20145/1
NDA
04-04-1995
20145/2
NDA
04-04-1995
20145/3
NDA
04-04-1995
20145/4
NDA
04-04-1995
20145/5
NDA
04-04-1995
20145/6
NDA
04-04-1995
18531/1
NDA
01-01-1982
74992/4
75076/1
74559/4
ANDA
ANDA
ANDA
12-11-1999
06-02-1998
75115/1
ANDA
10-08-2004
74992/3
75073/1
74559/3
ANDA
ANDA
ANDA
12-11-1999
30-08-1996
203693/1
ANDA
16-10-2017
208191/1
ANDA
26-08-2016
206391/1
ANDA
19-09-2017
203693/2
ANDA
16-10-2017
208191/2
ANDA
26-08-2016
206391/2
ANDA
19-09-2017
75115/2
ANDA
10-08-2004
74559/2
75075/1
74992/2
ANDA
ANDA
ANDA
30-08-1996
12-11-1999
203693/3
ANDA
16-10-2017
208191/3
ANDA
26-08-2016
206391/3
ANDA
19-09-2017
74559/1
74992/1
ANDA
ANDA
30-08-1996
12-11-1999
87355/1
ANDA
08-07-1988
71203/1
70077/1
ANDA
ANDA
08-05-1987
13-12-1985
72034/1
ANDA
24-05-1988
71492/1
ANDA
24-05-1988
70634/1
70633/1
ANDA
ANDA
19-06-1986
19-06-1986
18774/1
NDA
19-01-1983
18672/1
NDA
30-08-1983
21134/1
NDA
01-05-2000
21134/2
NDA
01-05-2000
21134/3
NDA
01-05-2000
18588/1
NDA
01-01-1982
70872/1
70871/1
ANDA
ANDA
08-01-1987
08-01-1987
18588/2
70863/1
NDA
ANDA
23-12-1983
08-01-1987
21359/1
NDA
21-06-2011
20144/2
20144/1
20144/5
20144/4
20144/3
NDA
NDA
NDA
NDA
NDA
27-02-1996
27-02-1996
27-02-1996
27-02-1996
27-02-1996
18537/2
NDA
16-06-1983
18537/1
NDA
01-01-1982
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Europe

Austria (6)
X
Product
Pack
Reg. Nr.
Reg. Type
Reg. Date
Reg. Valid
Revocation
Company
1-22443
17-03-1998
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Belgium (19)
X
Product
Pack
Market
Pres.
Dosage
ATC
Company
30x
-
transdermal
C01DA02
30x
N
transdermal
C01DA02
30x
-
transdermal
C01DA02
30x
Y
transdermal
C01DA02
30x
-
transdermal
C01DA02
30x
Y
transdermal
C01DA02
30x
Y
transdermal
C01DA02
30x
60x
Y
-

transdermal
C01DA02
30x
60x
Y
-

transdermal
C01DA02
30x
60x
Y
-

transdermal
C01DA02
30x
7x
Y
-

transdermal
C01DA02
30x
7x
Y
-

transdermal
C01DA02
30x
7x
Y
-

transdermal
C01DA02
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.

Croatia (1)
X
Product
Pack
Market
Pres.
Dosage
ATC
Company
14,4 ml otopina u bočici odmjernim susta
Y
Rx
-
C01DA02
Product
Pack
Reg. Nr.
Reg. Type
Reg. Date
Reg. Valid
Revocation
Company
14,4 ml otopina u bočici odmjernim susta
HR-H-453122375-01
14-11-2016
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Czechia (6)
X
Product
Pack
Market
Pres.
Dosage
ATC
Company
1MG/ML 10X10ML
1MG/ML 10X25ML
1MG/ML 10X50ML
1MG/ML 10X5ML
1MG/ML 1X50ML
Y
N
N
N
Y
iv
C01DA02
0,5MG 20
Y
oromucosal
C01DA02
0,4MG/DÁV 10G I
0,4MG/DÁV 10G II
Y
N
oromucosal
C01DA02
2,6MG 60
Y
oral
C01DA02
1MG/ML 10X10ML
1MG/ML 1X50ML
Y
N
iv
C01DA02
1MG/ML 10X10ML
Y
iv
C01DA02
Product
Pack
Reg. Nr.
Reg. Type
Reg. Date
Reg. Valid
Revocation
Company
1MG/ML 10X10ML
1MG/ML 10X25ML
1MG/ML 10X50ML
1MG/ML 10X5ML
1MG/ML 1X50ML
83/1071/94-C
83/1071/94-C
83/1071/94-C
83/1071/94-C
83/1071/94-C
NP
NP
NP
NP
NP
0,4MG/DÁV 10G I
0,4MG/DÁV 10G II
83/ 022/98-C
83/ 022/98-C
NP
NP
2,6MG 60
83/ 419/99-C
NP
1MG/ML 10X10ML
1MG/ML 1X50ML
83/ 048/91-S/C
83/ 048/91-S/C
NP
NP
1MG/ML 10X10ML
83/ 048/91-S/C
NP
Product
Pack
Ex-fact
Wholesale
Net retail
Gr. retail
Company
1MG/ML 10X10ML
1MG/ML 10X25ML
1MG/ML 10X50ML
1MG/ML 10X5ML
1MG/ML 1X50ML
0
0
0
0
0

0,4MG/DÁV 10G I
0,4MG/DÁV 10G II
67,5
67,5
101,72
101,72
1MG/ML 10X10ML
1MG/ML 1X50ML
0
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.

Denmark (7)
X
Product
Pack
Reg. Nr.
Reg. Type
Reg. Date
Reg. Valid
Revocation
Company
28100740376
MRP
01-08-1977
28100740476
MRP
01-08-1977
28103638903
PI
17-05-2004
28103851805
MRP
02-06-2006
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 (14)
X
Product
Pack
Market
Pres.
Dosage
ATC
Company
15x
30x
N
N
Rx
Rx
transdermal
C01DA02
15x
30x
N
N
Rx
Rx
transdermal
C01DA02
15x
30x
N
N
Rx
Rx
transdermal
C01DA02
10x10ml amp
10x25ml amp
1x50ml vial
Y
N
N
Rx
Rx
Rx
parenteral
C01DA02
30x sachet
Y
Rx
transdermal
C01DA02
30x sachet
Y
Rx
transdermal
C01DA02
30x sachet
Y
Rx
transdermal
C01DA02
1x15,4g container
Y
OTC
oromucosal
C01DA02
30x sachet
Y
Rx
transdermal
C01DA02
60x glass
Y
Rx
oral
C01DA02
30x sachet
Y
Rx
transdermal
C01DA02
60x glass
N
Rx
oral
C01DA02
1x10g al container
1x10g container (coc)
Y
Y
OTC
OTC
oromucosal
C01DA02
1x30g al tube
Y
Rx
topical
C01DA02
Product
Pack
Reg. Nr.
Reg. Type
Reg. Date
Reg. Valid
Revocation
Company
15x
30x
OGYI-T-08926/03
OGYI-T-08926/04
06-06-2003
06-06-2003
15x
30x
OGYI-T-08926/05
OGYI-T-08926/06
06-06-2003
06-06-2003
15x
30x
OGYI-T-08926/01
OGYI-T-08926/02
10x10ml amp
10x25ml amp
1x50ml vial
OGYI-T-05333/02
OGYI-T-05333/03
OGYI-T-05333/01
26-11-1996
26-11-1996
26-11-1996
30x sachet
OGYI-T-01291/02
01-01-1987
30x sachet
OGYI-T-01291/03
12-10-1995
1x15,4g container
OGYI-T-05683/01
01-01-1997
30x sachet
OGYI-T-10967/07
07-01-2000
60x glass
OGYI-T-10967/02
16-07-1984
30x sachet
OGYI-T-10967/06
60x glass
OGYI-T-10967/03
14-07-1999
1x10g al container
1x10g container (coc)
OGYI-T-10967/05
OGYI-T-10967/04
01-01-1988
01-01-1988
1x30g al tube
OGYI-T-20200/01
05-09-2006
Product
Pack
Ex-fact
Wholesale
Net retail
Gr. retail
Company
10x10ml amp
10x25ml amp
1x50ml vial
3756
9264
1715
3921,26
9671,62
1800,75
4627
10662
2161
4858
11195
2269
30x sachet
1961
2059,05
2471
2595
30x sachet
2789
2911,72
3494
3669
30x sachet
1577
1655,85
2001
2101
30x sachet
2268
2368
2842
2984
60x glass
630
670,95
825
866
30x sachet
1826
1917,3
2301
2416
60x glass
0
0
0
0
1x10g al container
1x10g container (coc)
586
586
626
626
770
770
809
809
1x30g al tube
10590
11055,96
12046
12648
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Iceland (2)
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 (16)
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.

Lithuania (10)
X
Product
Pack
Market
Pres.
Dosage
ATC
Company
50 ml N1 bottle
N10 - 5 ml bottle
Rx
Rx
iv
C01DA02
10 ml N10 amp
25 ml N10 amp
5 ml N10 amp
50 ml N10 bottle
Rx
Rx
Rx
Rx
iv
C01DA02
10 ml N10 amp
50 ml N1 bottle
Rx
Rx
iv
C01DA02
N25 bottle
Rx
sublingual
C01DA02
N25 bottle
Rx
sublingual
C01DA02
N20 blister
Rx
sublingual
C01DA02
11,2 g, 200 dozių N1 bottle
Rx
sublingual
C01DA02
N60 bottle
Rx
oral
C01DA02
180 išpurškimų N1 bottle
Rx
sublingual
C01DA02
N100 bottle
N25 bottle
Rx
Rx
oral
C01DA02
Product
Pack
Reg. Nr.
Reg. Type
Reg. Date
Reg. Valid
Revocation
Company
50 ml N1 bottle
N10 - 5 ml bottle
LT/L/18/0754/001
LT/L/18/0754/002
PI
PI
24-10-2018
24-10-2018
10 ml N10 amp
25 ml N10 amp
5 ml N10 amp
50 ml N10 bottle
LT/1/97/2909/002
LT/1/97/2909/003
LT/1/97/2909/001
LT/1/97/2909/004
NP
NP
NP
NP
11-02-1997
11-02-1997
11-02-1997
11-02-1997
10 ml N10 amp
50 ml N1 bottle
LT/1/97/2410/002
LT/1/97/2410/001
NP
NP
09-04-1997
09-04-1997
N25 bottle
LT/1/95/0855/001
NP
04-10-1995
N25 bottle
LT/1/95/0855/002
NP
04-10-1995
N20 blister
LT/1/01/2088/001
NP
04-07-2001
11,2 g, 200 dozių N1 bottle
LT/1/93/0105/001
NP
16-04-1993
N60 bottle
LT/1/95/1732/001
NP
10-05-1995
180 išpurškimų N1 bottle
LT/1/95/1732/002
NP
29-03-1996
N100 bottle
N25 bottle
LT/1/94/1674/002
LT/1/94/1674/001
NP
NP
21-11-1994
21-11-1994
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Malta (19)
X
Product
Pack
Reg. Nr.
Reg. Type
Reg. Date
Reg. Valid
Revocation
Company
MA806/00202
29-03-2006
MA806/00201
29-03-2006
MA1249/02602
29-11-2005
MA097/00101
10-10-2006
PI282/00101A
30-09-2014
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Poland (5)
X
Product
Pack
Market
Pres.
Dosage
ATC
Company
10 amp 2,5 ml
10 amp 2,5 ml
10 amp 5 ml
50 amp 2,5 ml
50 amp 2,5 ml
50 amp 5 ml
Lz
Lz
Lz
Lz
-
C01DA02
1 tube 30 g
Rp
-
C01DA02
1 poj. 10 g (180 dawek)
1 poj. 11 g (200 dawek)
1 poj. 11 g (200 dawek)
Rp
Rp
Rp
-
C01DA02
1 vial 50 ml
10 amp 10 ml
Lz
Lz
-
C01DA02
100 tabs
25 tabs
30 tabs
30 tabs (2x15)
Rp
Rp
Rp
-
C01DA02
Product
Pack
Reg. Nr.
Reg. Type
Reg. Date
Reg. Valid
Revocation
Company
10 amp 2,5 ml
10 amp 2,5 ml
10 amp 5 ml
50 amp 2,5 ml
50 amp 2,5 ml
50 amp 5 ml
07662
07661
07661
07662
07661
07661
NP
NP
NP
NP
NP
NP
17-10-2017
17-10-2017
17-10-2017
17-10-2017
17-10-2017
17-10-2017
1 poj. 10 g (180 dawek)
1 poj. 11 g (200 dawek)
1 poj. 11 g (200 dawek)
01568
01568
01568
NP
NP
NP
1 vial 50 ml
10 amp 10 ml
02649
02649
NP
NP
100 tabs
25 tabs
30 tabs
30 tabs (2x15)
01830
01830
01830
01830
NP
NP
NP
NP
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 (5)
X
Product
Pack
Market
Pres.
Dosage
ATC
Company
10 plicuri alcatuite din patru straturi
-
P6L
-
C01DA02
2 blister PVC-PVDC/Al x 10 tabs sublingu
-
P6L
-
C01DA02
x 1 flacon din plastic x 10g (180 doze)
x 1 flacon din Al x 10g (180 doze) subl
-
-
P6L
P6L
-
C01DA02
x 1 flac. x 60 tabs elib. prel.
-
P6L
-
C01DA02
10 fiole a cate 10 ml sol. perf.
-
PR
-
C01DA02
Product
Pack
Reg. Nr.
Reg. Type
Reg. Date
Reg. Valid
Revocation
Company
10 plicuri alcatuite din patru straturi
-
2 blister PVC-PVDC/Al x 10 tabs sublingu
-
x 1 flacon din plastic x 10g (180 doze)
x 1 flacon din Al x 10g (180 doze) subl
-
-
x 1 flac. x 60 tabs elib. prel.
-
10 fiole a cate 10 ml sol. perf.
-
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 (26)
X
Product
Pack
Market
Pres.
Dosage
ATC
Company
stekleničko 100 tabs
N
Rx
sublingual
C01DA02
1 vial 50 ml sol
-
-
C01DA02
30 transdermalnimi patch
-
-
C01DA02
30 transdermalnimi patch
-
-
C01DA02
30 transdermalnimi patch
-
-
C01DA02
28 patch
N
Rx
transdermal
C01DA02
28 patch
N
Rx
transdermal
C01DA02
28 patch
N
Rx
transdermal
C01DA02
30 bukalet 2 mg
-
Rx
sublingual
C01DA02
30 bukalet 5 mg
-
Rx
sublingual
C01DA02
10 patch 50 mg
-
Rx
transdermal
C01DA02
10 patch vrečkah
N
Rx
transdermal
C01DA02
15 transdermalnimi patch
N
-
C01DA02
15 transdermalnimi patch
N
-
C01DA02
15 transdermalnimi patch
N
-
C01DA02
2 vsebnikoma (z zaporko mehanskim pršiln
-
Rx
sublingual
C01DA02
steklenico 13,2 g sol za 200 razprškov
N
Rx
sublingual
C01DA02
10 amp 25 ml sol
10 amp 5 ml sol
-
-
Rx
Rx
parenteral
C01DA02
1 vial 50 ml sol
N
Rx
iv
C01DA02
50 tabs 6,5 mg
-
Rx
oral
C01DA02
stekleničko 100 tabs
stekleničko 25 tabs
-
-
Rx
Rx
oral
C01DA02
plastenko 25 tabs
-
Rx
oral
C01DA02
plastenko 25 tabs
-
Rx
oral
C01DA02
Product
Pack
Reg. Nr.
Reg. Type
Reg. Date
Reg. Valid
Revocation
Company
stekleničko 100 tabs
103-44/2018-3
NP
07-06-2018
07-06-2018
07-06-2018
1 vial 50 ml sol
/
-
20-04-2016
20-04-2017
1 vial 50 ml sol
/
-
23-05-2016
23-05-2017
30 transdermalnimi patch
842-128/2019
-
17-04-2019
17-04-2020
30 transdermalnimi patch
842-127/2019
-
17-04-2019
17-04-2020
30 transdermalnimi patch
842-129/2019
-
23-04-2019
23-04-2020
10 amp 50 ml sol
/
-
08-12-2015
07-12-2016
28 patch
103-6/2018-4
NP
11-04-2018
11-04-2018
06-10-2019
28 patch
103-6/2018-4
NP
11-04-2018
11-04-2018
06-10-2019
28 patch
103-6/2018-4
NP
11-04-2018
11-04-2018
06-10-2019
10 patch vrečkah
5363-I-1093/11
NP
21-06-2011
15 transdermalnimi patch
842-301/2019
-
07-08-2019
07-08-2020
15 transdermalnimi patch
842-240/2018
-
06-07-2018
06-07-2019
15 transdermalnimi patch
842-240/2018
-
06-07-2018
06-07-2019
2 vsebnikoma (z zaporko mehanskim pršiln
-
steklenico 13,2 g sol za 200 razprškov
10023-125/2017-12
NP
10-05-2018
10 amp 25 ml sol
10 amp 5 ml sol
-
-
1 vial 50 ml sol
5363-I-50/12
NP
18-01-2012
50 tabs 6,5 mg
-
stekleničko 100 tabs
stekleničko 25 tabs
-
-
plastenko 25 tabs
-
plastenko 25 tabs
-
Product
Pack
Ex-fact
Wholesale
Net retail
Gr. retail
Company
30 transdermalnimi patch
16,99
30 transdermalnimi patch
21,44
30 transdermalnimi patch
13,38
2 vsebnikoma (z zaporko mehanskim pršiln
steklenico 13,2 g sol za 200 razprškov
5,96
10 amp 25 ml sol
10 amp 5 ml sol
50 tabs 6,5 mg
stekleničko 100 tabs
stekleničko 25 tabs
plastenko 25 tabs
plastenko 25 tabs
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 (42)
X
Product
Pack
Market
Pres.
Dosage
ATC
Company
30 parches
Y
Rx
transdermal
C01DA02
30 parches
-
Rx
transdermal
C01DA02
30 parches
Y
Rx
transdermal
C01DA02
15 parches
30 parches
-
Y
Rx
Rx
transdermal
C01DA02
15 parches
30 parches
-
Y
Rx
Rx
transdermal
C01DA02
15 parches
30 parches
-
Y
Rx
Rx
transdermal
C01DA02
30 parches
-
Rx
transdermal
C01DA02
30 parches
-
Rx
transdermal
C01DA02
30 parches
-
Rx
transdermal
C01DA02
15 parches
30 parches
-
Y
Rx
Rx
transdermal
C01DA02
15 parches
30 parches
-
Y
Rx
Rx
transdermal
C01DA02
15 parches
30 parches
-
Y
Rx
Rx
transdermal
C01DA02
30 parches
7 parches
Y
-
Rx
Rx
transdermal
C01DA02
30 parches
7 parches
Y
-
Rx
Rx
transdermal
C01DA02
30 parches
7 parches
Y
-
Rx
Rx
transdermal
C01DA02
30 parches
7 parches
-
-
Rx
Rx
transdermal
C01DA02
30 parches
7 parches
-
-
Rx
Rx
transdermal
C01DA02
30 parches
7 parches
-
-
Rx
Rx
transdermal
C01DA02
30 parches
-
Rx
transdermal
C01DA02
30 parches
-
Rx
transdermal
C01DA02
30 parches
-
Rx
transdermal
C01DA02
30 parches
-
Rx
transdermal
C01DA02
30 parches
-
Rx
transdermal
C01DA02
30 parches
7 parches
Y
-
Rx
Rx
transdermal
C01DA02
30 parches
Y
Rx
transdermal
C01DA02
30 parches
7 parches
Y
Y
Rx
Rx
transdermal
C01DA02
30 parches
7 parches
Y
Y
Rx
Rx
transdermal
C01DA02
30 parches
7 parches
Y
Y
Rx
Rx
transdermal
C01DA02
30 parches
7 parches
Y
Y
Rx
Rx
transdermal
C01DA02
30 parches
500 parches
7 parches
Y
Y
-
Rx
Rx
Rx
transdermal
C01DA02
30 parches
500 parches
7 parches
Y
Y
-
Rx
Rx
Rx
transdermal
C01DA02
30 parches
500 parches
7 parches
Y
Y
-
Rx
Rx
Rx
transdermal
C01DA02
1 tube of 30 g
Y
Rx
rectal
C05AE01
12 amp of 5 ml
Y
Rx
iv
C01DA02
1 envase pulverizador of 200 dosis
Y
Rx
sublingual
C01DA02
30 tabs
-
Rx
sublingual
C01DA02
Product
Pack
Reg. Nr.
Reg. Type
Reg. Date
Reg. Valid
Revocation
Company
30 parches
60314
01-11-1994
30 parches
62265
01-03-1999
30 parches
60313
01-11-1994
15 parches
30 parches
63682
63682
19-02-2001
19-02-2001
15 parches
30 parches
63683
63683
16-02-2001
16-02-2001
15 parches
30 parches
63681
63681
16-02-2001
16-02-2001
30 parches
57943
01-09-1988
30 parches
60274
01-03-1994
30 parches
57942
01-09-1988
15 parches
30 parches
63677
63677
20-02-2001
20-02-2001
15 parches
30 parches
63678
63678
20-02-2001
20-02-2001
15 parches
30 parches
63676
63676
20-02-2001
20-02-2001
30 parches
7 parches
59989
59989
01-02-1994
01-02-1994
30 parches
7 parches
59990
59990
01-02-1994
01-02-1994
30 parches
7 parches
59988
59988
01-02-1994
01-02-1994
30 parches
7 parches
57394
57394
01-10-1987
01-10-1987
30 parches
7 parches
61877
61877
01-02-1998
01-02-1998
30 parches
7 parches
57395
57395
01-10-1987
01-10-1987
30 parches
7 parches
57359
57359
01-07-1987
01-07-1987
30 parches
61449
01-05-1997
30 parches
7 parches
57358
57358
01-07-1987
01-07-1987
30 parches
7 parches
71210
71210
17-07-2009
17-07-2009
30 parches
7 parches
71214
71214
17-07-2009
17-07-2009
30 parches
7 parches
71209
71209
17-07-2009
17-07-2009
30 parches
500 parches
7 parches
58567
58567
58567
01-04-1991
01-04-1991
01-04-1991
30 parches
500 parches
7 parches
62264
62264
62264
01-11-1998
01-11-1998
01-11-1998
30 parches
500 parches
7 parches
58568
58568
58568
01-04-1991
01-04-1991
01-04-1991
1 tube of 30 g
68286
31-01-2007
12 amp of 5 ml
55332
01-12-1980
12 amp of 10 ml
57127
01-11-1987
1 envase pulverizador of 200 dosis
56574
01-08-1985
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 (32)
X
Product
Pack
Market
Pres.
Dosage
ATC
Company
Product
Pack
Reg. Nr.
Reg. Type
Reg. Date
Reg. Valid
Revocation
Company
Nationell decentral eller ömsesidig
06-03-1998
PI
28-12-2001
31-12-2005
PI
PI
PI
PI
22-10-2003
03-04-2019
26-10-2016
22-05-2003
30-06-2008
30-06-2008
Nationell decentral eller ömsesidig
19-12-1994
31-01-2018
Nationell decentral eller ömsesidig
19-12-1994
31-01-2018
Nationell decentral eller ömsesidig
19-12-1994
31-01-2018
Nationell decentral eller ömsesidig
28-04-2014
Nationell decentral eller ömsesidig
08-06-2011
31-03-2012
Nationell decentral eller ömsesidig
08-06-2011
31-03-2012
Nationell decentral eller ömsesidig
03-12-1975
30-06-2019
Nationell decentral eller ömsesidig
03-12-1975
30-06-2019
PI
PI
26-06-2003
26-06-2003
29-02-2008
29-02-2008
PI
PI
PI
PI
PI
06-11-2019
17-12-2019
23-06-2004
04-11-2004
23-06-2004
30-06-2008
30-06-2008
30-06-2008
PI
PI
PI
28-05-2007
28-05-2007
28-05-2007
31-12-2007
31-01-2009
31-01-2009
Nationell decentral eller ömsesidig
08-10-1993
Nationell decentral eller ömsesidig
19-10-1979
30-11-2014
Nationell decentral eller ömsesidig
22-11-1935
30-11-2014
Nationell decentral eller ömsesidig
18-08-2006
PI
PI
22-08-2008
22-08-2008
31-12-2011
31-12-2011
PI
27-10-2009
28-02-2014
Nationell decentral eller ömsesidig
13-06-1986
Nationell decentral eller ömsesidig
13-06-1986
Nationell decentral eller ömsesidig
21-06-1983
Nationell decentral eller ömsesidig
21-06-1983
Nationell decentral eller ömsesidig
22-11-1995
28-02-2009
Nationell decentral eller ömsesidig
22-11-1995
28-02-2009
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 (14)
X
Product
Pack
Reg. Nr.
Reg. Type
Reg. Date
Reg. Valid
Revocation
Company
45986 4
45986 4
45986 4
Hauptzulassung
Hauptzulassung
Hauptzulassung
08-03-1984
08-03-1984
08-03-1984
07-03-2024
07-03-2024
07-03-2024
45986 3
45986 3
45986 3
Hauptzulassung
Hauptzulassung
Hauptzulassung
08-03-1984
08-03-1984
08-03-1984
07-03-2024
07-03-2024
07-03-2024
51920 2
Hauptzulassung
22-01-1993
31-12-2022
51920 1
51920 1
Hauptzulassung
Hauptzulassung
22-01-1993
22-01-1993
31-12-2022
31-12-2022
44192 2
44192 2
Hauptzulassung
Hauptzulassung
07-12-1981
07-12-1981
26-04-2022
26-04-2022
44192 3
Exportzulassung
07-12-1981
26-04-2022
44192 1
44192 1
44192 1
Hauptzulassung
Hauptzulassung
Hauptzulassung
07-12-1981
07-12-1981
07-12-1981
26-04-2022
26-04-2022
26-04-2022
56398 1
Hauptzulassung
15-01-2010
55459 2
Hauptzulassung
25-04-2001
26-04-2022
55459 1
Hauptzulassung
25-04-2001
26-04-2022
36830 1
Hauptzulassung
05-11-1971
26-04-2022
40558 2
Hauptzulassung
28-11-1977
29-04-2022
45371 1
45371 1
Hauptzulassung
Hauptzulassung
06-04-1984
06-04-1984
07-03-2024
07-03-2024
58099 1
Hauptzulassung
31-10-2007
30-10-2022
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.