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

isosorbide dinitrate

North America

Canada (3)
X
Product
Pack
Market
Pres.
Dosage
ATC
Company
Ethical
oral
C01DA08
Ethical
oral
C01DA08
Ethical
sublingual
C01DA08
Product
Pack
Reg. Nr.
Reg. Type
Reg. Date
Reg. Valid
Revocation
Company
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United States (42)
X
Product
Pack
Market
Pres.
Dosage
ATC
Company
N
N
N


oral
C01DA08
N
N
N


sublingual
C01DA08
N
oral
C01DA08
N
oral
C01DA08
Y
Rx
oral
C01DA08
Y
Rx
oral
C01DA08
N
N

sublingual
C01DA08
N
sublingual
C01DA08
Y
N
Rx
sublingual
C01DA08
N
sublingual
C01DA08
N
N

sublingual
C01DA08
Product
Pack
Reg. Nr.
Reg. Type
Reg. Date
Reg. Valid
Revocation
Company
12093/6
12093/5
12093/2
NDA
NDA
NDA
29-07-1988
29-07-1988
29-07-1988
12940/5
12940/4
12940/3
NDA
NDA
NDA
29-07-1988
29-07-1988
29-07-1988
12882/2
NDA
29-07-1988
12882/1
NDA
29-07-1988
12093/1
NDA
29-07-1988
12093/7
NDA
29-07-1988
86033/1
86031/1
ANDA
ANDA
26-02-1988
29-09-1987
86066/1
ANDA
29-10-1987
86925/1
ANDA
12-03-1987
86223/1
ANDA
07-01-1988
87545/1
86169/1
ANDA
ANDA
18-09-1986
19-09-1986
89191/1
ANDA
17-02-1987
86054/1
ANDA
29-10-1987
86225/1
ANDA
19-02-1988
88088/1
ANDA
02-11-1987
87537/1
ANDA
02-10-1987
89367/1
ANDA
07-04-1988
86167/1
ANDA
19-09-1986
89192/1
ANDA
17-02-1987
40591/1
ANDA
10-01-2007
87946/1
ANDA
12-01-1988
87564/1
ANDA
18-09-1986
40723/1
ANDA
17-03-2008
86067/1
86055/1
ANDA
ANDA
29-10-1987
02-11-1987
86923/1
ANDA
12-03-1987
86222/1
86221/1
ANDA
ANDA
19-02-1988
07-01-1988
86168/1
86166/2
ANDA
ANDA
18-09-1986
19-09-1986
89190/1
ANDA
17-02-1987
86034/1
ANDA
06-01-1988
16776/3
NDA
01-04-1996
16192/2
NDA
01-04-1996
16191/2
NDA
01-04-1996
86405/2
ANDA
21-08-1990
88124/1
ANDA
21-08-1990
88125/1
ANDA
21-08-1990
16776/2
NDA
01-04-1996
16192/1
16191/1
NDA
NDA
01-04-1996
01-04-1996
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Europe

Austria (0)
No result.
Belgium (5)
X
Product
Pack
Market
Pres.
Dosage
ATC
Company
100x
N
oral
C01DA08
100x
Y
oral
C01DA08
100x
N
oral
C01DA08
180x
60x
Y
Y

oral/sublingual
C01DA08
Product
Pack
Reg. Nr.
Reg. Type
Reg. Date
Reg. Valid
Revocation
Company
100x
BE123496
-
100x
BE115166
-
100x
BE135843
-
180x
60x
BE025566
BE025566
-
-
Product
Pack
Ex-fact
Wholesale
Net retail
Gr. retail
Company
180x
60x
3,66
1,53
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Croatia (1)
X
Product
Pack
Market
Pres.
Dosage
ATC
Company
40 (4x10) sublingvalnih tabs in blister
Y
Rx
-
C01DA08
Product
Pack
Reg. Nr.
Reg. Type
Reg. Date
Reg. Valid
Revocation
Company
40 (4x10) sublingvalnih tabs in blister
20-12-2012
20-12-2017
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Czechia (11)
X
Product
Pack
Market
Pres.
Dosage
ATC
Company
120MG 20 I
120MG 20 II
120MG 30 I
120MG 30 II
120MG 50 I
120MG 50 II
N
N
N
N
N
N
oral
C01DA08
120MG 20 I
120MG 20 II
120MG 30 I
120MG 30 II
120MG 50 I
120MG 50 II
N
N
Y
N
N
N
oral
C01DA08
20MG 100 I
20MG 100 II
20MG 20 I
20MG 20 II
20MG 50 I
20MG 50 II
N
N
N
N
N
N
oral
C01DA08
20MG 100 I
20MG 100 II
20MG 20 I
20MG 20 II
20MG 50 I
20MG 50 II
N
N
Y
N
N
N
oral
C01DA08
40MG 50 I
40MG 50 II
N
N
oral
C01DA08
40MG 50 I
40MG 50 II
Y
N
oral
C01DA08
1MG/ML 10X10ML
1MG/ML 1X100ML
1MG/ML 1X50ML
Y
N
N
intracoronary/iv
C01DA08
1MG/ML 10X10ML
N
intracoronary/iv
C01DA08
1MG/ML 1X100ML
1MG/ML 1X50ML
N
N
intracoronary/iv
C01DA08
1,25MG/DÁV 1X15ML
Y
sublingual
C01DA08
375MG/15ML 1X15ML
Y
sublingual
C01DA08
Product
Pack
Reg. Nr.
Reg. Type
Reg. Date
Reg. Valid
Revocation
Company
120MG 20 I
120MG 20 II
120MG 30 I
120MG 30 II
120MG 50 I
120MG 50 II
83/ 112/87-C
83/ 112/87-C
83/ 112/87-C
83/ 112/87-C
83/ 112/87-C
83/ 112/87-C
NP
NP
NP
NP
NP
NP
120MG 20 I
120MG 20 II
120MG 30 I
120MG 30 II
120MG 50 I
120MG 50 II
83/ 112/87-C
83/ 112/87-C
83/ 112/87-C
83/ 112/87-C
83/ 112/87-C
83/ 112/87-C
NP
NP
NP
NP
NP
NP
20MG 100 I
20MG 100 II
20MG 20 I
20MG 20 II
20MG 50 I
20MG 50 II
83/ 233/80-C
83/ 233/80-C
83/ 233/80-C
83/ 233/80-C
83/ 233/80-C
83/ 233/80-C
NP
NP
NP
NP
NP
NP
20MG 100 I
20MG 100 II
20MG 20 I
20MG 20 II
20MG 50 I
20MG 50 II
83/ 233/80-C
83/ 233/80-C
83/ 233/80-C
83/ 233/80-C
83/ 233/80-C
83/ 233/80-C
NP
NP
NP
NP
NP
NP
40MG 50 I
40MG 50 II
83/ 135/84-C
83/ 135/84-C
NP
NP
40MG 50 I
40MG 50 II
83/ 135/84-C
83/ 135/84-C
NP
NP
1MG/ML 10X10ML
1MG/ML 1X100ML
1MG/ML 1X50ML
83/ 244/80-C
83/ 131/87-C
83/ 131/87-C
NP
NP
NP
1MG/ML 10X10ML
83/ 244/80-C
NP
1MG/ML 1X100ML
1MG/ML 1X50ML
83/ 131/87-C
83/ 131/87-C
NP
NP
1,25MG/DÁV 1X15ML
83/ 242/80-C
NP
375MG/15ML 1X15ML
83/ 242/80-C
NP
Product
Pack
Ex-fact
Wholesale
Net retail
Gr. retail
Company
120MG 20 I
120MG 20 II
120MG 30 I
120MG 30 II
120MG 50 I
120MG 50 II
0
0
163,04
0
0
0
245,13
120MG 20 I
120MG 20 II
120MG 30 I
120MG 30 II
120MG 50 I
120MG 50 II
0
0
163,04
0
0
0
245,13
20MG 100 I
20MG 100 II
20MG 20 I
20MG 20 II
20MG 50 I
20MG 50 II
0
0
0
0
0
0
20MG 100 I
20MG 100 II
20MG 20 I
20MG 20 II
20MG 50 I
20MG 50 II
0
0
0
0
0
0
40MG 50 I
40MG 50 II
77,02
0
116,07
40MG 50 I
40MG 50 II
77,02
0
116,07
1MG/ML 10X10ML
1MG/ML 1X100ML
1MG/ML 1X50ML
0
0
0

1MG/ML 1X100ML
1MG/ML 1X50ML
0
0
1,25MG/DÁV 1X15ML
154,44
232,55
375MG/15ML 1X15ML
154,44
232,55
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Denmark (1)
X
Product
Pack
Market
Pres.
Dosage
ATC
Company
Product
Pack
Reg. Nr.
Reg. Type
Reg. Date
Reg. Valid
Revocation
Company
28101184184
NP
07-02-1985
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Hungary (0)
No result.
Iceland (0)
No result.
Ireland (1)
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
N20 blister
N50 blister
Rx
Rx
oral
C01DA08
N20 blister
N50 blister
Rx
Rx
oral
C01DA08
N50 blister
Rx
oral
C01DA08
N50 blister
Rx
oral
C01DA08
10 ml N10 amp
Rx
iv/intraarterial
C01DA08
15 ml (su dosing pump), 300 dozių N1 bot
Rx
oromucosal
C01DA08
Product
Pack
Reg. Nr.
Reg. Type
Reg. Date
Reg. Valid
Revocation
Company
N20 blister
N50 blister
LT/1/97/3140/001
LT/1/97/3140/002
NP
NP
09-04-1997
09-04-1997
N20 blister
N50 blister
LT/1/97/3140/003
LT/1/97/3140/004
NP
NP
09-04-1997
09-04-1997
N50 blister
LT/1/95/1381/001
NP
05-04-1995
N50 blister
LT/1/95/1381/002
NP
05-04-1995
10 ml N10 amp
LT/1/97/3142/001
NP
09-04-1997
15 ml (su dosing pump), 300 dozių N1 bot
LT/1/97/3142/002
NP
09-04-1997
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 (0)
No result.
Romania (2)
X
Product
Pack
Market
Pres.
Dosage
ATC
Company
x 10 blister Al/PVC x 10 tabs
x 100 blister Al/PVC x 10 tabs
x 3 blister Al/PVC x 10 tabs
-
-
-
P-6L
P-6L/S
P-6L
-
C01DA08
3 blister PVC-PVDC/Al x 20 tabs
-
P6L
-
C01DA08
Product
Pack
Reg. Nr.
Reg. Type
Reg. Date
Reg. Valid
Revocation
Company
x 10 blister Al/PVC x 10 tabs
x 100 blister Al/PVC x 10 tabs
x 3 blister Al/PVC x 10 tabs
-
-
-
3 blister PVC-PVDC/Al x 20 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.

Slovenia (4)
X
Product
Pack
Market
Pres.
Dosage
ATC
Company
50 caps (5 x 10 caps blister)
-
Rx
oral
C01DA08
40 tablet 5 mg
-
Rx
oral
C01DA08
20 tablet 20 mg
-
Rx
oral
C01DA08
40 tabs (4 x 10 tabs blister)
-
Rx
sublingual
C01DA08
Product
Pack
Reg. Nr.
Reg. Type
Reg. Date
Reg. Valid
Revocation
Company
50 caps (5 x 10 caps blister)
-
40 tablet 5 mg
-
20 tablet 20 mg
-
40 tabs (4 x 10 tabs blister)
-
Product
Pack
Ex-fact
Wholesale
Net retail
Gr. retail
Company
50 caps (5 x 10 caps blister)
40 tablet 5 mg
20 tablet 20 mg
40 tabs (4 x 10 tabs blister)
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Spain (3)
X
Product
Pack
Market
Pres.
Dosage
ATC
Company
50 tabs
Y
Rx
oral
C01DA08
20 tabs
50 tabs
-
-
Rx
Rx
oral
C01DA08
30 tabs
-
Rx
oral
C01DA08
Product
Pack
Reg. Nr.
Reg. Type
Reg. Date
Reg. Valid
Revocation
Company
50 tabs
49679
01-12-1971
20 tabs
50 tabs
48987
48987
01-04-1970
01-04-1970
30 tabs
57081
01-09-1986
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 (4)
X
Product
Pack
Market
Pres.
Dosage
ATC
Company
Rx
-
C01DA08
Rx
-
C01DA08
Rx
-
C01DA08
Rx
-
C01DA08
Product
Pack
Reg. Nr.
Reg. Type
Reg. Date
Reg. Valid
Revocation
Company
Nationell decentral eller ömsesidig
05-02-1988
31-01-2018
Nationell decentral eller ömsesidig
21-06-1983
31-01-2018
Nationell decentral eller ömsesidig
08-05-1987
31-01-2018
Nationell decentral eller ömsesidig
21-11-1963
31-01-2018
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Switzerland (7)
X
Product
Pack
Reg. Nr.
Reg. Type
Reg. Date
Reg. Valid
Revocation
Company
39387 1
Hauptzulassung
25-06-1976
41390 1
Hauptzulassung
16-08-1979
30-03-2024
38470 1
Hauptzulassung
08-01-1982
45979 2
Hauptzulassung
30-12-1983
30-03-2024
35797 6
35797 6
Hauptzulassung
Hauptzulassung
08-06-1970
08-06-1970
35797 7
Hauptzulassung
08-06-1970
35797 8
Hauptzulassung
08-06-1970
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