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

diatrizoic acid

North America

Canada (1)
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 (38)
X
Product
Pack
Market
Pres.
Dosage
ATC
Company
N
INJECTION
V08AA01
N
INJECTION
V08AA01
N
INJECTION
V08AA01
N
INJECTION
V08AA01
Y
Rx
urethral
V08AA01
Y
Rx
urethral
V08AA01
Y
Rx
oral/rectal
V08AA01
N
oral/rectal
V08AA01
N
INJECTION
V08AA01
N
INJECTION
V08AA01
N
oral/rectal
V08AA01
N
INJECTION
V08AA01
N
INJECTION
V08AA01
N
INJECTION
V08AA01
N
INJECTION
V08AA01
N
INJECTION
V08AA01
N
INJECTION
V08AA01
Y
Rx
oral/rectal
V08AA01
N
urethral
V08AA01
N
INJECTION
V08AA01
N
INJECTION
V08AA01
N
INJECTION
V08AA01
N
INJECTION
V08AA01
N
INJECTION
V08AA01
N
INJECTION
V08AA01
N
INJECTION
V08AA01
N
urethral
V08AA01
N
INJECTION
V08AA01
Product
Pack
Reg. Nr.
Reg. Type
Reg. Date
Reg. Valid
Revocation
Company
87726/1
ANDA
23-09-1982
87724/1
ANDA
23-09-1982
87723/1
ANDA
23-09-1982
11620/2
NDA
01-01-1982
10040/18
NDA
01-01-1982
10040/22
NDA
09-11-1982
10040/17
NDA
01-01-1982
11245/3
NDA
01-01-1982
87728/1
ANDA
23-09-1982
11386/1
NDA
01-01-1982
9561/3
NDA
01-01-1982
16403/2
NDA
01-01-1982
11386/3
NDA
01-01-1982
9561/1
NDA
01-01-1982
16403/1
NDA
01-01-1982
86505/1
ANDA
01-01-1982
16403/3
NDA
01-01-1982
10220/3
NDA
01-01-1982
10220/2
NDA
01-01-1982
87075/1
ANDA
01-01-1982
87074/1
ANDA
01-01-1982
87073/1
ANDA
01-01-1982
19292/1
NDA
29-09-1989
10040/21
NDA
01-01-1982
10040/16
NDA
01-01-1982
10040/12
NDA
01-01-1982
89347/1
ANDA
01-06-1988
10040/6
NDA
01-01-1982
10040/1
NDA
01-01-1982
10040/20
NDA
01-01-1982
10040/19
NDA
01-01-1982
87729/1
ANDA
23-09-1982
87731/1
ANDA
23-09-1982
87739/1
ANDA
23-09-1982
87725/1
ANDA
23-09-1982
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Europe

Austria (6)
X
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Belgium (1)
X
Product
Pack
Market
Pres.
Dosage
ATC
Company
250 mL
250 mL
Y
N

iv
V08AA01
Product
Pack
Reg. Nr.
Reg. Type
Reg. Date
Reg. Valid
Revocation
Company
250 mL
250 mL
BE098402
BE098402
-
-
Product
Pack
Ex-fact
Wholesale
Net retail
Gr. retail
Company
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Croatia (0)
No result.
Czechia (0)
No result.
Denmark (1)
X
Product
Pack
Market
Pres.
Dosage
ATC
Company
Product
Pack
Reg. Nr.
Reg. Type
Reg. Date
Reg. Valid
Revocation
Company
28101536392
NP
18-01-1993
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Hungary (1)
X
Product
Pack
Market
Pres.
Dosage
ATC
Company
10x100ml glass
5x100ml glass
Y
N
Rx
Rx
oral
V08AA01
Product
Pack
Reg. Nr.
Reg. Type
Reg. Date
Reg. Valid
Revocation
Company
10x100ml glass
5x100ml glass
OGYI-T-00686/02
OGYI-T-00686/01
01-01-1970
01-01-1970
Product
Pack
Ex-fact
Wholesale
Net retail
Gr. retail
Company
10x100ml glass
5x100ml glass
24985
12492
26084,34
13041,65
27074
14032
28428
14734
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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 (2)
X
Product
Pack
Market
Pres.
Dosage
ATC
Company
ampulė (20 ml), N10 amp
Rx
iv
V08AA01
100 ml N10 bottle
20 ml N10 amp
Rx
Rx
iv
V08AA01
Product
Pack
Reg. Nr.
Reg. Type
Reg. Date
Reg. Valid
Revocation
Company
ampulė (20 ml), N10 amp
LT/1/95/1062/001
NP
04-10-1995
100 ml N10 bottle
20 ml N10 amp
LT/1/95/1062/003
LT/1/95/1062/002
NP
NP
04-10-1995
04-10-1995
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Malta (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.

Poland (3)
X
Product
Pack
Market
Pres.
Dosage
ATC
Company
1 bottle 100 ml
10 butelek 100 ml
5 butelek 100 ml
Rp
Rp
Rp
-
V08AA01
1 bottle 100 ml
10 butelek po 100 ml
5 butelek po 100 ml
Rp
Rp
Rp
-
V08AA01
1 bottle 100 ml
10 butelek 100 ml
5 butelek 100 ml
Rp
Rp
Rp
-
V08AA01
Product
Pack
Reg. Nr.
Reg. Type
Reg. Date
Reg. Valid
Revocation
Company
1 bottle 100 ml
10 butelek 100 ml
5 butelek 100 ml
906/12
906/12
906/12
PI
PI
PI
27-12-2022
27-12-2022
27-12-2022
1 bottle 100 ml
10 butelek po 100 ml
5 butelek po 100 ml
42/14
42/14
42/14
PI
PI
PI
30-01-2019
30-01-2019
30-01-2019
1 bottle 100 ml
10 butelek 100 ml
5 butelek 100 ml
06813
06813
06813
NP
NP
NP
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Romania (0)
No result.
Slovenia (5)
X
Product
Pack
Market
Pres.
Dosage
ATC
Company
1 stekleničko 100 ml sol
10 stekleničkami 100 ml sol
-
-

-
V08AA01
stekleničko 100 ml sol
-
-
V08AA01
10 amp 20 ml sol
-
Rx
parenteral
V08AA01
5 ampul 20 ml (60%)
steklenička 100 ml (60%)
-
-
Rx
Rx
parenteral
V08AA01
5 ampul 20ml (75%)
steklenička po100ml (75%)
-
-
Rx
Rx
parenteral
V08AA01
Product
Pack
Reg. Nr.
Reg. Type
Reg. Date
Reg. Valid
Revocation
Company
1 stekleničko 100 ml sol
10 stekleničkami 100 ml sol
/
/
-
-
19-09-2015
24-02-2015
18-09-2016
24-02-2016
stekleničko 100 ml sol
842-486/2019
-
13-01-2020
13-01-2021
10 amp 20 ml sol
-
5 ampul 20 ml (60%)
steklenička 100 ml (60%)
-
-
5 ampul 20ml (75%)
steklenička po100ml (75%)
-
-
Product
Pack
Ex-fact
Wholesale
Net retail
Gr. retail
Company
1 stekleničko 100 ml sol
10 stekleničkami 100 ml sol
5 ampul 20 ml (60%)
steklenička 100 ml (60%)
5 ampul 20ml (75%)
steklenička po100ml (75%)
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 (6)
X
Product
Pack
Market
Pres.
Dosage
ATC
Company
1 bottle of 100 ml
Y
Rx
oral/rectal
V08AA01
1 vial of 20 ml
1 vial of 50 ml
-
-
Rx
Rx
iv
V08AA01
1 bottle of 100 ml
1 bottle of 250 ml
-
-
Rx
Rx
iv
V08AA01
1 bottle of 100 ml
1 bottle of 250 ml
Y
Y
Rx
Rx
iv
V08AA01
1 vial of 100 ml
1 vial of 20 ml
1 vial of 50 ml
-
Y
Y
Rx
Rx
Rx
iv
V08AA01
1 amp of 20 ml
1 bottle of 100 ml
1 bottle of 50 ml
Y
Y
Y
Rx
Rx
Rx
iv
V08AA01
Product
Pack
Reg. Nr.
Reg. Type
Reg. Date
Reg. Valid
Revocation
Company
1 bottle of 100 ml
36270
01-06-1961
1 vial of 20 ml
1 vial of 50 ml
27961
27961
01-09-1957
01-09-1957
1 bottle of 100 ml
1 bottle of 250 ml
50928
50928
01-02-1973
01-02-1973
1 bottle of 100 ml
1 bottle of 250 ml
80974
80974
17-06-2016
17-06-2016
1 vial of 100 ml
1 vial of 20 ml
1 vial of 50 ml
51331
51331
51331
01-06-1973
01-06-1973
01-06-1973
1 amp of 20 ml
1 bottle of 100 ml
1 bottle of 50 ml
23817
23817
23817
01-06-1955
01-06-1955
01-06-1955
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Sweden (4)
X
Product
Pack
Reg. Nr.
Reg. Type
Reg. Date
Reg. Valid
Revocation
Company
Nationell decentral eller ömsesidig
24-02-1964
Nationell decentral eller ömsesidig
09-02-1968
31-07-2006
Nationell decentral eller ömsesidig
28-02-1964
30-04-2008
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.

Switzerland (2)
X
Product
Pack
Market
Pres.
Dosage
ATC
Company
-
-
B
B
-
V08AA01
Product
Pack
Reg. Nr.
Reg. Type
Reg. Date
Reg. Valid
Revocation
Company
27620 1
27620 1
Hauptzulassung
Hauptzulassung
07-06-1961
07-06-1961
02-10-2023
02-10-2023
62509 1
62509 1
Hauptzulassung
Hauptzulassung
20-12-2012
20-12-2012
19-12-2022
19-12-2022
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