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

cromoglicic acid

North America

Canada (4)
X
Product
Pack
Market
Pres.
Dosage
ATC
Company
OTC
OPHTHALMIC
S01GX01
OTC
OPHTHALMIC
S01GX01
Product
Pack
Reg. Nr.
Reg. Type
Reg. Date
Reg. Valid
Revocation
Company
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United States (30)
X
Product
Pack
Market
Pres.
Dosage
ATC
Company
N
oral
A07EB01
Y
Rx
oral
A07EB01
N
inh
R03BC01
Product
Pack
Reg. Nr.
Reg. Type
Reg. Date
Reg. Valid
Revocation
Company
74443/1
ANDA
30-01-1995
202745/1
ANDA
04-04-2013
75067/1
ANDA
19-07-1999
75585/1
ANDA
21-12-2000
75333/1
ANDA
30-04-2002
74209/1
ANDA
26-04-1994
75175/1
ANDA
30-09-1999
75271/1
ANDA
18-01-2000
76469/1
ANDA
17-06-2005
75346/1
ANDA
25-10-1999
74706/1
ANDA
29-04-1998
75615/1
ANDA
26-01-2001
75282/1
ANDA
16-06-1999
19188/1
NDA
22-12-1989
20479/1
NDA
29-02-1996
16990/1
NDA
01-01-1982
18596/1
NDA
28-05-1982
20463/1
NDA
03-01-1997
18155/1
NDA
03-10-1984
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Europe

Austria (5)
X
Product
Pack
Reg. Nr.
Reg. Type
Reg. Date
Reg. Valid
Revocation
Company
1-24846
17-02-2003
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Belgium (10)
X
Product
Pack
Market
Pres.
Dosage
ATC
Company
0,3 mL
0,3 mL
Y
-

ocular
S01GX01
10 mL
Y
ocular
S01GX01
10 mL
5 mL
Y
-

ocular
S01GX01
2 mL
N
inh
R03BC01
13,5 mL
-
nasal
R01AC01
15 mL
-
nasal
R01AC01
10 mL
Y
ocular
S01GX01
Product
Pack
Reg. Nr.
Reg. Type
Reg. Date
Reg. Valid
Revocation
Company
0,3 mL
0,3 mL
BE467022
BE467022
-
-
10 mL
5 mL
BE531546
BE531546
-
-
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Croatia (1)
X
Product
Pack
Market
Pres.
Dosage
ATC
Company
10 jednodoznih spremnika u sachet
20 jednodoznih spremnika u sachet
N
N
OTC
OTC
-
S01GX01
Product
Pack
Reg. Nr.
Reg. Type
Reg. Date
Reg. Valid
Revocation
Company
10 jednodoznih spremnika u sachet
20 jednodoznih spremnika u sachet
HR-H-586030470-01
HR-H-586030470-02
25-10-2019
25-10-2019
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Czechia (8)
X
Product
Pack
Market
Pres.
Dosage
ATC
Company
20MG/ML 10X0,3ML
20MG/ML 20X0,3ML
N
Y
ocular
S01GX01
20MG/ML+2,8MG/0,14ML 10ML+15ML
Y
ocular/nasal
S01GX01
20MG/ML 1X15ML
20MG/ML 2X15ML
Y
N
nasal
R01AC01
40MG/ML 1X10ML
40MG/ML 1X5ML
40MG/ML 2X5ML
40MG/ML 3X5ML
Y
N
N
N
ocular
S01GX01
100MG 100
Y
oral
A07EB01
Product
Pack
Reg. Nr.
Reg. Type
Reg. Date
Reg. Valid
Revocation
Company
20MG/ML 10X0,3ML
20MG/ML 20X0,3ML
64/ 212/15-C
64/ 212/15-C
MRP/DCP
MRP/DCP
20MG/ML 1X15ML
20MG/ML 2X15ML
24/ 141/96-C
24/ 141/96-C
NP
NP
40MG/ML 1X10ML
40MG/ML 1X5ML
40MG/ML 2X5ML
40MG/ML 3X5ML
64/ 382/17-C
64/ 382/17-C
64/ 382/17-C
64/ 382/17-C
MRP/DCP
MRP/DCP
MRP/DCP
MRP/DCP
100MG 100
14/ 305/89-S/C
NP
Product
Pack
Ex-fact
Wholesale
Net retail
Gr. retail
Company
20MG/ML 10X0,3ML
20MG/ML 20X0,3ML
0
0
20MG/ML 1X15ML
20MG/ML 2X15ML
68,81
0
103,7
40MG/ML 1X10ML
40MG/ML 1X5ML
40MG/ML 2X5ML
40MG/ML 3X5ML
0
0
0
0
100MG 100
446,31
645,07
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Denmark (8)
X
Product
Pack
Reg. Nr.
Reg. Type
Reg. Date
Reg. Valid
Revocation
Company
28101496092
NP
05-03-1993
28101502292
NP
05-03-1993
28105382714
DCP
18-03-2015
28101001578
NP
10-06-1982
28104596809
PI
21-01-2010
28100924177
NP
26-04-1978
28103801177
NP
26-04-1978
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Hungary (6)
X
Product
Pack
Market
Pres.
Dosage
ATC
Company
1x10ml container
1x10ml container hdpe cap és kupakot véd
Y
Y
OTC
OTC
-
S01GX01
10x container
20x container
N
Y
OTC
OTC
ocular
S01GX01
1x10ml ldpe bottle
1x5ml ldpe bottle
2x5ml ldpe bottle
3x5ml ldpe bottle
Y
N
N
N
OTC
OTC
OTC
OTC
-
S01GX01
1x10ml plastic container hdpe cap
1x10ml plastic container pp cap
Y
Y
OTC
OTC
-
S01GX01
1x10ml container (pe)
Y
OTC
ocular
S01GX01
1x15g glass
Y
OTC
nasal
R01AC01
Product
Pack
Reg. Nr.
Reg. Type
Reg. Date
Reg. Valid
Revocation
Company
1x10ml container
1x10ml container hdpe cap és kupakot véd
OGYI-T-22584/01
OGYI-T-22584/04
05-12-2013
05-12-2013
10x container
20x container
OGYI-T-22584/02
OGYI-T-22584/03
30-10-2014
30-10-2014
1x10ml ldpe bottle
1x5ml ldpe bottle
2x5ml ldpe bottle
3x5ml ldpe bottle
OGYI-T-23368/04
OGYI-T-23368/01
OGYI-T-23368/02
OGYI-T-23368/03
22-03-2018
22-03-2018
22-03-2018
22-03-2018
1x10ml plastic container hdpe cap
1x10ml plastic container pp cap
OGYI-T-03691/02
OGYI-T-03691/01
01-01-1987
01-01-1987
1x10ml container (pe)
OGYI-T-04037/01
01-01-1994
1x15g glass
OGYI-T-03798/01
01-09-1991
Product
Pack
Ex-fact
Wholesale
Net retail
Gr. retail
Company
1x10ml container
1x10ml container hdpe cap és kupakot véd
0
0
0
0
0
0
0
0
10x container
20x container
0
0
0
0
0
0
0
0
1x10ml ldpe bottle
1x5ml ldpe bottle
2x5ml ldpe bottle
3x5ml ldpe bottle
0
0
0
0
0
0
0
0
0
0
0
0
0
0
0
0
1x10ml plastic container hdpe cap
1x10ml plastic container pp cap
0
0
0
0
0
0
0
0
1x10ml container (pe)
0
0
0
0
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Iceland (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.

Ireland (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.

Lithuania (4)
X
Product
Pack
Market
Pres.
Dosage
ATC
Company
10 ml N1 bottle
OTC
ocular
S01GX01
5 ml N1 bottle
OTC
ocular
S01GX01
0,2 ml N20 single dose container
0,2 ml N60 single dose container
OTC
OTC
ocular
S01GX01
10 ml N1 bottle
5 ml N1 bottle
5 ml N2 bottle
5 ml N3 bottle
OTC
OTC
OTC
OTC
ocular
S01GX01
Product
Pack
Reg. Nr.
Reg. Type
Reg. Date
Reg. Valid
Revocation
Company
10 ml N1 bottle
LT/1/96/2408/001
NP
29-03-1996
5 ml N1 bottle
LT/1/96/2408/002
NP
29-03-1996
0,2 ml N20 single dose container
0,2 ml N60 single dose container
LT/1/96/2408/004
LT/1/96/2408/005
NP
NP
29-03-1996
29-03-1996
10 ml N1 bottle
5 ml N1 bottle
5 ml N2 bottle
5 ml N3 bottle
LT/1/15/3711/004
LT/1/15/3711/001
LT/1/15/3711/002
LT/1/15/3711/003
DCP
DCP
DCP
DCP
22-04-2015
22-04-2015
22-04-2015
22-04-2015
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Malta (10)
X
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Poland (11)
X
Product
Pack
Market
Pres.
Dosage
ATC
Company
10 poj. jednodawkowych
20 poj. jednodawkowych
OTC
OTC
-
S01GX01
1 bottle 10 ml
OTC
-
S01GX01
1 bottle 10 ml
OTC
-
S01GX01
1 poj. 15 ml
2 poj. 15 ml
OTC
-
R01AC01
1 bottle 10 ml
1 fl. 5 ml
20 poj. 0,5 ml
50 poj. 0,5 ml
OTC
OTC
-
S01GX01
1 bottle 10 ml
Rp
-
S01GX01
1 bottle 10 ml
Rp
-
S01GX01
1 bottle 10 ml
1 bottle 5 ml
2 butelki 5 ml
3 butelki 5 ml
OTC
OTC
OTC
OTC
-
S01GX01
1 bottle 5 ml
1 fl. 10 ml
1 zestaw: 2 butelki 5 ml
OTC
OTC
-
S01GX01
1 bottle 10 ml
OTC
-
S01GX01
Product
Pack
Reg. Nr.
Reg. Type
Reg. Date
Reg. Valid
Revocation
Company
10 poj. jednodawkowych
20 poj. jednodawkowych
22656
22656
DCP
DCP
1 bottle 10 ml
08980
NP
1 poj. 15 ml
2 poj. 15 ml
03464
03464
NP
NP
1 bottle 10 ml
1 fl. 5 ml
20 poj. 0,5 ml
50 poj. 0,5 ml
03527
03527
03527
03527
NP
NP
NP
NP
1 bottle 10 ml
01878
NP
1 bottle 10 ml
421/11
PI
18-10-2021
1 bottle 10 ml
1 bottle 5 ml
2 butelki 5 ml
3 butelki 5 ml
24616
24616
24616
24616
MRP
MRP
MRP
MRP
13-03-2023
13-03-2023
13-03-2023
13-03-2023
1 bottle 5 ml
1 fl. 10 ml
1 zestaw: 2 butelki 5 ml
03484
03484
03484
NP
NP
NP
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Romania (3)
X
Product
Pack
Market
Pres.
Dosage
ATC
Company
x 1 flac. PEID, prevazut cu aplicator pt
-
P-6L
-
R01AC01
x 1 flac. PEID, prevazut cu aplicator pt
-
P-6L
-
S01GX01
1 flac. din PEJD de culoare alba prevazu
1 flac. din PEJD de culoare alba prevazu
2 flac. din PEJD de culoare alba prevazu
3 flac. din PEJD de culoare alba prevazu
-
-
-
-
P6L
P6L
P6L
P6L
-
S01GX01
Product
Pack
Reg. Nr.
Reg. Type
Reg. Date
Reg. Valid
Revocation
Company
x 1 flac. PEID, prevazut cu aplicator pt
-
x 1 flac. PEID, prevazut cu aplicator pt
-
1 flac. din PEJD de culoare alba prevazu
1 flac. din PEJD de culoare alba prevazu
2 flac. din PEJD de culoare alba prevazu
3 flac. din PEJD de culoare alba prevazu
-
-
-
-
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Slovenia (4)
X
Product
Pack
Market
Pres.
Dosage
ATC
Company
50 caps za inhalacijo 20 mg
-
Rx
ocular
R03BC01
50 ampul 2 ml (20 mg/2 ml)
-
Rx
inh
R03BC01
vdihovalnik inhalacijsko suspenzijo pod
-
Rx
inh
R03BC01
stekleničko 10 ml sol (40mg/1ml) kapalni
-
Rx
ocular
S01GX01
Product
Pack
Reg. Nr.
Reg. Type
Reg. Date
Reg. Valid
Revocation
Company
50 ampul 2 ml (20 mg/2 ml)
-
vdihovalnik inhalacijsko suspenzijo pod
-
stekleničko 10 ml sol (40mg/1ml) kapalni
-
Product
Pack
Ex-fact
Wholesale
Net retail
Gr. retail
Company
50 ampul 2 ml (20 mg/2 ml)
vdihovalnik inhalacijsko suspenzijo pod
stekleničko 10 ml sol (40mg/1ml) kapalni
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Spain (6)
X
Product
Pack
Market
Pres.
Dosage
ATC
Company
1 bottle of 10 ml
-
OTC
ocular
S01GX01
1 bottle of 15 ml
-
Rx
nasal
R01AC01
1 bottle of 10 ml
Y
Rx
ocular
S01GX01
20 envases unidosis
Y
OTC
ocular
S01GX01
Product
Pack
Reg. Nr.
Reg. Type
Reg. Date
Reg. Valid
Revocation
Company
1 bottle of 10 ml
65867
27-01-2004
1 bottle of 15 ml
57869
01-09-1988
20 envases unidosis
80267
18-12-2015
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Sweden (24)
X
Product
Pack
Reg. Nr.
Reg. Type
Reg. Date
Reg. Valid
Revocation
Company
Nationell decentral eller ömsesidig
27-06-2013
Nationell decentral eller ömsesidig
04-06-2004
30-04-2009
Nationell decentral eller ömsesidig
30-10-2014
31-10-2018
Nationell decentral eller ömsesidig
29-11-1991
18-12-2019
Nationell decentral eller ömsesidig
06-05-1994
Nationell decentral eller ömsesidig
06-05-1994
Nationell decentral eller ömsesidig
19-11-2015
PI
16-11-2001
31-03-2006
Nationell decentral eller ömsesidig
12-11-1971
31-07-2019
Nationell decentral eller ömsesidig
14-04-1978
Nationell decentral eller ömsesidig
04-12-1992
Nationell decentral eller ömsesidig
17-03-1989
31-10-2006
PI
22-02-2002
31-12-2006
PI
29-05-1998
31-12-2006
Nationell decentral eller ömsesidig
07-11-1986
Nationell decentral eller ömsesidig
28-04-1976
30-09-2004
Nationell decentral eller ömsesidig
09-06-1989
Nationell decentral eller ömsesidig
10-02-2017
Nationell decentral eller ömsesidig
04-12-1992
31-03-2008
Nationell decentral eller ömsesidig
04-12-1992
30-09-2004
Nationell decentral eller ömsesidig
14-03-1997
31-12-2012
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 (6)
X
Product
Pack
Market
Pres.
Dosage
ATC
Company
-
-
D
D
-
S01GX01
-
B
-
A07EB01
Product
Pack
Reg. Nr.
Reg. Type
Reg. Date
Reg. Valid
Revocation
Company
55670 1
Hauptzulassung
05-07-2002
11-02-2022
55898 1
Exportzulassung
18-09-2001
15-07-2022
53534 1
53534 1
Hauptzulassung
Hauptzulassung
03-10-1996
03-10-1996
51386 1
Hauptzulassung
19-06-1992
01-10-2022
44778 1
Hauptzulassung
29-09-1982
49232 1
49232 1
Hauptzulassung
Hauptzulassung
24-06-1988
24-06-1988
05-09-2022
05-09-2022
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