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

barium sulfate with suspending agents

North America

Canada (0)
No result.
United States (12)
X
Product
Pack
Reg. Nr.
Reg. Type
Reg. Date
Reg. Valid
Revocation
Company
208143/1
NDA
15-01-2016
208143/5
NDA
04-08-2017
208844/1
NDA
14-10-2016
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Europe

Austria (5)
X
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Belgium (0)
No result.
Croatia (0)
No result.
Czechia (2)
X
Product
Pack
Market
Pres.
Dosage
ATC
Company
1G/ML 1X2000ML
Y
gastroenteral
V08BA01
50MG/ML 150ML
50MG/ML 1X2000ML
N
Y
gastroenteral
V08BA01
Product
Pack
Reg. Nr.
Reg. Type
Reg. Date
Reg. Valid
Revocation
Company
1G/ML 1X2000ML
48/ 150/82-C
NP
50MG/ML 150ML
50MG/ML 1X2000ML
48/ 300/91-C
48/ 300/91-C
NP
NP
Product
Pack
Ex-fact
Wholesale
Net retail
Gr. retail
Company
1G/ML 1X2000ML
352,88
517,63
50MG/ML 150ML
50MG/ML 1X2000ML
0
640,67
903,98
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Denmark (0)
No result.
Hungary (3)
X
Product
Pack
Market
Pres.
Dosage
ATC
Company
1x2000ml bottle
Y
Rx
oral
V08BA01
1x150ml bottle
N
Rx
oral
V08BA01
1x150g tube
1x800g tube
N
N
Rx
Rx
topical
V08BA01
Product
Pack
Reg. Nr.
Reg. Type
Reg. Date
Reg. Valid
Revocation
Company
1x2000ml bottle
OGYI-T-01128/01
01-01-1983
1x150ml bottle
OGYI-T-01636/01
01-01-1991
1x150g tube
1x800g tube
OGYI-T-01129/02
OGYI-T-01129/01
01-01-1983
01-01-1983
Product
Pack
Ex-fact
Wholesale
Net retail
Gr. retail
Company
1x150g tube
1x800g tube
0
0
0
0
0
0
0
0
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Iceland (0)
No result.
Ireland (1)
X
Product
Pack
Market
Pres.
Dosage
ATC
Company
Y
Rx
Powder for oral/rectal suspension
V08BA01
Product
Pack
Reg. Nr.
Reg. Type
Reg. Date
Reg. Valid
Revocation
Company
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Lithuania (1)
X
Product
Pack
Market
Pres.
Dosage
ATC
Company
200 ml, N1 bottle
200 ml, N24 bottle
Rx
Rx
oral/rectal
V08BA01
Product
Pack
Reg. Nr.
Reg. Type
Reg. Date
Reg. Valid
Revocation
Company
200 ml, N1 bottle
200 ml, N24 bottle
LT/1/95/0786/002
LT/1/95/0786/001
NP
NP
22-11-1995
22-11-1995
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Malta (3)
X
Product
Pack
Market
Pres.
Dosage
ATC
Company
Product
Pack
Reg. Nr.
Reg. Type
Reg. Date
Reg. Valid
Revocation
Company
AA1344/00101
15-01-2019
MA053/00101
28-08-2006
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Poland (1)
X
Product
Pack
Market
Pres.
Dosage
ATC
Company
1 bottle 240 ml
1 bottle 250 ml
1 op. 200 ml
Lz
Lz
Lz
-
V08BA01
Product
Pack
Reg. Nr.
Reg. Type
Reg. Date
Reg. Valid
Revocation
Company
1 bottle 240 ml
1 bottle 250 ml
1 op. 200 ml
02765
02765
02765
NP
NP
NP
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Romania (1)
X
Product
Pack
Market
Pres.
Dosage
ATC
Company
x 1 flac. din PE x 135 g pulb. pt. susp.
x 1 flac. din PE x 95 g pulb. pt. susp.
-
-
S/P-RF
S/P-RF
-
V08BA01
Product
Pack
Reg. Nr.
Reg. Type
Reg. Date
Reg. Valid
Revocation
Company
x 1 flac. din PE x 135 g pulb. pt. susp.
x 1 flac. din PE x 95 g pulb. pt. susp.
-
-
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Slovenia (13)
X
Product
Pack
Market
Pres.
Dosage
ATC
Company
34 x 340 g powd lončku (96,805 g/100g)
-
Rx
oral
V08BA01
polietilenska steklenica 2000 ml suspenz
-
-
V08BA01
polietilenska steklenica 2000 ml suspenz
-
Rx
rectal
V08BA01
1 lonček 400 g powd
-
-
V08BA01
1 steklenica 2000 ml suspenzije
N
-
V08BA01
tubo 150 g paste
-
-
V08BA01
24 vrečkami 397 g powd
-
-
V08BA01
plastenka 5 l susp (0,6 g/ml)
-
Rx
oral
V08BA01
vrečka 400 g powd (940,15mg/1g), cevka i
-
Rx
oral
V08BA01
1 PVC vrečka praškom
N
-
V08BA01
skodelica 340 g powd (984,5mg/1g)
-
Rx
oral
V08BA01
Product
Pack
Reg. Nr.
Reg. Type
Reg. Date
Reg. Valid
Revocation
Company
34 x 340 g powd lončku (96,805 g/100g)
-
polietilenska steklenica 2000 ml suspenz
/
-
18-06-2009
18-06-2010
polietilenska steklenica 2000 ml suspenz
-
1 lonček 400 g powd
/
-
01-08-2013
01-08-2014
1 steklenica 2000 ml suspenzije
842-331/2019
-
20-08-2019
20-08-2020
tubo 150 g paste
/
-
20-01-2010
20-01-2011
tubo 150 g paste
842-58/2019
-
21-02-2019
21-02-2020
24 vrečkami 397 g powd
/
-
18-05-2011
18-05-2012
plastenka 5 l susp (0,6 g/ml)
-
vrečka 400 g powd (940,15mg/1g), cevka i
-
1 PVC vrečka praškom
842-439/2018
-
27-12-2018
27-12-2019
skodelica 340 g powd (984,5mg/1g)
-
Product
Pack
Ex-fact
Wholesale
Net retail
Gr. retail
Company
34 x 340 g powd lončku (96,805 g/100g)
polietilenska steklenica 2000 ml suspenz
polietilenska steklenica 2000 ml suspenz
1 steklenica 2000 ml suspenzije
38,29
24 vrečkami 397 g powd
plastenka 5 l susp (0,6 g/ml)
vrečka 400 g powd (940,15mg/1g), cevka i
1 PVC vrečka praškom
22,63
skodelica 340 g powd (984,5mg/1g)
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 (11)
X
Product
Pack
Market
Pres.
Dosage
ATC
Company
1 enema
10 enemas
Y
Y
Rx
Rx
rectal
V08BA01
1 envase unidosis of 340 g
10 envases unidosis of 340 g
Y
Y
Rx
Rx
oral
V08BA01
30 sobres
Y
Rx
oral
V08BA01
20 frascos unidosis of 750 ml conteniend
4 frascos multidosis of 2000 ml
Y
Y
Rx
Rx
oral/rectal
V08BA01
5 bolsas of 800 g
Y
Rx
VÍA RECTAL, VÍA ORAL
V08BA01
4 frascos multidosis of 2000 ml
Y
Rx
oral/rectal
V08BA01
23 envases unidosis of 340 g
Y
Rx
oral
V08BA01
1 enema
-
Rx
rectal
V08BA01
1 envase unidosis of 340 g
-
Rx
oral
V08BA01
30 sobres
-
Rx
oral
V08BA01
Product
Pack
Reg. Nr.
Reg. Type
Reg. Date
Reg. Valid
Revocation
Company
1 enema
10 enemas
57393
57393
01-03-1988
01-03-1988
1 envase unidosis of 340 g
10 envases unidosis of 340 g
57391
57391
01-03-1988
01-03-1988
30 sobres
73640
15-03-2011
20 frascos unidosis of 750 ml conteniend
4 frascos multidosis of 2000 ml
73287
73287
17-01-2011
17-01-2011
5 bolsas of 800 g
73154
01-12-2010
4 frascos multidosis of 2000 ml
73212
20-12-2010
23 envases unidosis of 340 g
73215
20-12-2010
1 enema
81172
16-08-2016
1 envase unidosis of 340 g
81221
19-09-2016
30 sobres
81222
19-09-2016
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Sweden (3)
X
Product
Pack
Reg. Nr.
Reg. Type
Reg. Date
Reg. Valid
Revocation
Company
Nationell decentral eller ömsesidig
18-03-1988
31-01-2019
Nationell decentral eller ömsesidig
25-04-1986
30-04-2007
Nationell decentral eller ömsesidig
24-08-2007
31-05-2014
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 (4)
X
Product
Pack
Market
Pres.
Dosage
ATC
Company
-
B
-
V08BA01
-
B
-
V08BA01
Product
Pack
Reg. Nr.
Reg. Type
Reg. Date
Reg. Valid
Revocation
Company
43406 1
Exportzulassung
04-09-1981
19-09-2020
41341 1
Hauptzulassung
01-03-1977
11-12-2022
30241 2
Hauptzulassung
17-02-1964
08-12-2023
50151 1
Hauptzulassung
10-11-1989
05-02-2024
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.