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

triamcinolone

North America

Canada (13)
X
Product
Pack
Market
Pres.
Dosage
ATC
Company
Rx
INTRA-ARTICULAR, INTRABURSAL, INTRADERMAL, INTRASYNOVIAL
H02AB08
Rx
topical
D07AB09
Rx
intraarticular/periarticular/intrasynovial
H02AB08
Rx
intravitreal
S01BA05
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United States (177)
X
Product
Pack
Market
Pres.
Dosage
ATC
Company
N
INJECTION
H02AB08
N
topical
D07AB09
N
topical
D07AB09
N
topical
D07AB09
N
topical
D07AB09
N
topical
D07AB09
N
oral
H02AB08
N
INJECTION
H02AB08
N
oral
H02AB08
N
oral
H02AB08
N
oral
H02AB08
N
topical
D07AB09
N
N

topical
D07AB09
N
N

topical
D07AB09
N
N

topical
D07AB09
N
topical
D07AB09
N
N

topical
D07AB09
N
topical
D07AB09
Y
Rx
INJECTION
H02AB08
Y
Rx
INJECTION
H02AB08
N
topical
D07AB09
N
topical
D07AB09
N
topical
D07AB09
N
topical
D07AB09
N
topical
D07AB09
N
topical
D07AB09
N
N
N
N



topical
D07AB09
N
topical
D07AB09
Y
Rx
topical
D07AB09
N
topical
D07AB09
Y
Rx
INJECTION
H02AB08
Y
Rx
INJECTION
H02AB08
N
dental
A01AC01
N
topical
D07AB09
N
topical
D07AB09
N
topical
D07AB09
N
topical
D07AB09
N
N

oral
H02AB08
N
oral
H02AB08
N
N

oral
H02AB08
N
oral
H02AB08
N
oral
H02AB08
N
oral
H02AB08
N
N

oral
H02AB08
N
N

oral
H02AB08
N
N

topical
D07AB09
N
Y

Rx
topical
D07AB09
N
topical
D07AB09
N
topical
D07AB09
N
topical
D07AB09
Y
Rx
topical
D07AB09
Y
Rx
topical
D07AB09
Y
Rx
intravitreal
S01BA05
Y
Rx
intraocular
S01BA05
N
intraarticular/im/intravitreal
H02AB08
Product
Pack
Reg. Nr.
Reg. Type
Reg. Date
Reg. Valid
Revocation
Company
20120/1
NDA
04-02-2000
12802/1
NDA
01-01-1982
80745/2
ANDA
01-01-1982
83017/3
ANDA
01-01-1982
80750/4
ANDA
01-01-1982
83016/4
ANDA
01-01-1982
83015/2
ANDA
01-01-1982
11161/10
NDA
01-01-1982
11161/9
NDA
01-01-1982
11685/3
NDA
01-01-1982
11161/4
NDA
01-01-1982
11960/4
NDA
01-01-1982
11161/7
NDA
01-01-1982
11161/11
NDA
01-01-1982
80745/3
ANDA
01-01-1982
83017/4
88818/1
ANDA
ANDA
01-01-1982
16-10-1984
80750/3
88780/1
ANDA
ANDA
01-01-1982
01-10-1984
83016/5
88819/1
ANDA
ANDA
01-01-1982
16-10-1984
88781/1
ANDA
05-10-1984
88820/1
83015/3
ANDA
ANDA
16-10-1984
01-01-1982
83380/1
ANDA
01-01-1982
16466/2
NDA
01-01-1982
16466/1
NDA
01-01-1982
18117/1
NDA
23-04-1982
87375/1
ANDA
01-11-1988
85539/1
ANDA
01-01-1982
87377/1
ANDA
01-11-1988
85539/2
ANDA
01-01-1982
87376/1
ANDA
01-11-1988
85539/3
ANDA
01-01-1982
11283/3
NDA
01-01-1982
11283/8
NDA
01-01-1982
11283/6
NDA
01-01-1982
11283/10
NDA
01-01-1982
84343/1
11602/3
11602/1
84343/2
ANDA
NDA
NDA
ANDA
01-01-1982
01-01-1982
01-01-1982
01-01-1982
83944/1
ANDA
01-01-1982
12104/1
NDA
01-01-1982
83943/1
ANDA
01-01-1982
12097/1
NDA
01-01-1982
12041/1
NDA
01-01-1982
14901/1
NDA
01-01-1982
86240/1
ANDA
01-01-1982
71383/1
ANDA
06-07-1987
84908/1
ANDA
01-01-1982
84908/2
ANDA
01-01-1982
84908/3
ANDA
01-01-1982
87113/1
ANDA
01-01-1982
84318/1
84286/1
ANDA
ANDA
01-01-1982
01-01-1982
84406/1
ANDA
01-01-1982
84708/1
ANDA
01-01-1982
84319/1
84267/1
ANDA
ANDA
01-01-1982
01-01-1982
84340/1
ANDA
01-01-1982
83750/1
ANDA
01-01-1982
84709/1
ANDA
01-01-1982
85601/1
ANDA
01-01-1982
84775/1
ANDA
01-01-1982
85834/1
84270/1
ANDA
ANDA
01-01-1982
01-01-1982
84268/1
84320/1
ANDA
ANDA
01-01-1982
01-01-1982
84707/1
ANDA
01-01-1982
11600/3
11600/1
NDA
NDA
01-01-1982
01-01-1982
202374/1
ANDA
08-05-2013
40374/1
40040/1
ANDA
ANDA
05-06-2001
30-09-1994
207651/1
ANDA
26-12-2017
208763/1
ANDA
01-02-2017
40038/1
86277/1
ANDA
ANDA
26-10-1994
01-01-1982
78104/2
78104/1
ANDA
ANDA
14-11-2014
30-07-2009
202374/2
ANDA
08-05-2013
87799/1
ANDA
07-06-1982
85691/3
ANDA
01-01-1982
208320/1
ANDA
22-08-2017
87385/3
ANDA
01-01-1982
87902/1
40037/1
ANDA
ANDA
27-12-1982
30-09-1994
205373/1
ANDA
13-05-2016
206312/1
ANDA
11-08-2016
70730/1
ANDA
01-10-1986
207651/2
ANDA
26-12-2017
207117/1
ANDA
05-08-2016
208763/2
ANDA
01-02-2017
11601/6
NDA
01-01-1982
86413/3
86414/1
ANDA
ANDA
01-01-1982
40039/1
86276/1
ANDA
ANDA
26-11-1997
01-01-1982
208848/1
ANDA
18-09-2017
85691/2
ANDA
01-01-1982
206379/1
ANDA
22-07-2016
87385/1
ANDA
01-01-1982
40386/1
ANDA
05-06-2001
208590/1
ANDA
03-03-2017
207651/3
ANDA
26-12-2017
208763/3
ANDA
01-02-2017
86275/1
ANDA
01-01-1982
207550/1
ANDA
11-12-2017
85122/1
ANDA
01-01-1982
86394/1
ANDA
01-01-1982
85529/1
84072/1
ANDA
ANDA
01-01-1982
01-01-1982
87430/1
ANDA
01-11-1988
87429/1
ANDA
01-11-1988
87428/1
ANDA
01-11-1988
88042/2
ANDA
25-03-2015
88042/1
ANDA
19-03-1984
88042/3
ANDA
25-03-2015
22048/1
NDA
29-11-2007
22220/1
NDA
16-06-2008
88693/1
ANDA
02-08-1984
88196/1
ANDA
25-03-1983
88691/1
ANDA
02-08-1984
88197/1
ANDA
25-03-1983
88198/1
ANDA
25-03-1983
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Europe

Austria (14)
X
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Belgium (9)
X
Product
Pack
Market
Pres.
Dosage
ATC
Company
5 mL
N
intraarticular/intradermal
H02AB08
1 mL
1 mL
5 mL
-
-
-


im/intraarticular
H02AB08
2 mL
-
im/intraarticular
H02AB08
10 g
30 g
-
Y

cut
D07AB09
5 mL
Y
intraarticular/intradermal
H02AB08
1 mL
Y
intravitreal
S01BA05
Product
Pack
Reg. Nr.
Reg. Type
Reg. Date
Reg. Valid
Revocation
Company
1 mL
1 mL
5 mL
0166IS0318F012
0166IS0319F012
0166IS0318F012
-
-
-
10 g
30 g
BE090343
BE090343
-
-
120x
30x
BE190215
BE190215
-
-
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Croatia (2)
X
Product
Pack
Market
Pres.
Dosage
ATC
Company
5 amp 1 ml suspenzije in blister
Y
Rx
-
H02AB08
16,5 g suspenzije u bočici odmjernim sus
6,5 g suspenzije u bočici odmjernim sust
N
N
Rx
Rx
-
R01AD11
Product
Pack
Reg. Nr.
Reg. Type
Reg. Date
Reg. Valid
Revocation
Company
5 amp 1 ml suspenzije in blister
HR-H-363427938-01
20-12-2016
16,5 g suspenzije u bočici odmjernim sus
6,5 g suspenzije u bočici odmjernim sust
HR-H-444175872-02
HR-H-444175872-01
26-02-2018
26-02-2018
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Czechia (5)
X
Product
Pack
Market
Pres.
Dosage
ATC
Company
1MG/G+30MG/G 30G
Y
cut
D07XB02
55MCG/DÁV 120DÁV
55MCG/DÁV 30DÁV
N
N
nasal
R01AD11
20MG/ML 10X1ML
Y
IAT/PAT
H02AB08
Product
Pack
Reg. Nr.
Reg. Type
Reg. Date
Reg. Valid
Revocation
Company
1MG/G 10G
46/ 124/77-C
NP
1MG/G+30MG/G 30G
46/ 182/80-C
NP
55MCG/DÁV 120DÁV
55MCG/DÁV 30DÁV
69/ 324/15-C
69/ 324/15-C
MRP/DCP
MRP/DCP
20MG/ML 10X1ML
56/ 002/14-C
MRP/DCP
Product
Pack
Ex-fact
Wholesale
Net retail
Gr. retail
Company
55MCG/DÁV 120DÁV
55MCG/DÁV 30DÁV
0
0
20MG/ML 10X1ML
1594,05
2142,84
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Denmark (9)
X
Product
Pack
Reg. Nr.
Reg. Type
Reg. Date
Reg. Valid
Revocation
Company
28100583470
NP
25-08-1971
28105613815
DCP
10-08-2016
28104571909
DCP
13-04-2011
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Hungary (4)
X
Product
Pack
Market
Pres.
Dosage
ATC
Company
1x15g al tube
Y
Rx
topical
D07AB09
5x1ml amp
Y
Rx
parenteral
H02AB08
1x120adag hdpe container
1x30adag hdpe container
N
N
Rx
Rx
-
R01AD11
30x blister
30x glass +ldpe kupak
N
Y
Rx
Rx
oral
H02AB08
Product
Pack
Reg. Nr.
Reg. Type
Reg. Date
Reg. Valid
Revocation
Company
1x15g al tube
OGYI-T-03414/01
22-11-1971
5x1ml amp
OGYI-T-01198/01
01-01-1985
1x120adag hdpe container
1x30adag hdpe container
OGYI-T-22852/02
OGYI-T-22852/01
15-06-2015
15-06-2015
30x blister
30x glass +ldpe kupak
OGYI-T-00689/02
OGYI-T-00689/01
01-01-1970
01-01-1970
Product
Pack
Ex-fact
Wholesale
Net retail
Gr. retail
Company
1x15g al tube
696
741,24
912
958
5x1ml amp
3194
3334,54
4001
4201
1x120adag hdpe container
1x30adag hdpe container
0
0
0
0
0
0
0
0
30x blister
30x glass +ldpe kupak
0
929
0
989,39
0
1217
0
1278
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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
15-09-2003
15-09-2003
Product
Pack
Ex-fact
Wholesale
Net retail
Gr. retail
Company
1.617
18.239
1.617
18.239
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 (10)
X
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Lithuania (4)
X
Product
Pack
Market
Pres.
Dosage
ATC
Company
15 g N1 tube
Rx
cut
D07AB09
1 ml N5 amp
Rx
im/intraarticular
H02AB08
N50 blister
Rx
oral
H02AB08
120 išpurškimų N1 bottle
30 išpurškimų N1 bottle
Rx
Rx
nasal
R01AD11
Product
Pack
Reg. Nr.
Reg. Type
Reg. Date
Reg. Valid
Revocation
Company
15 g N1 tube
LT/1/94/0978/001
NP
22-06-1994
1 ml N5 amp
LT/1/94/2324/001
NP
21-11-1994
N50 blister
LT/1/95/2576/001
NP
04-10-1995
120 išpurškimų N1 bottle
30 išpurškimų N1 bottle
LT/1/15/3760/002
LT/1/15/3760/001
RP
RP
02-07-2015
02-07-2015
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Malta (4)
X
Product
Pack
Reg. Nr.
Reg. Type
Reg. Date
Reg. Valid
Revocation
Company
PI555/02901A
30-07-2013
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Poland (2)
X
Product
Pack
Market
Pres.
Dosage
ATC
Company
1 bottle 120 dawek
1 bottle 30 dawek
Rp
Rp
-
R01AD11
20 tabs blister
20 tabs w fiolce
Rp
Rp
-
H02AB08
Product
Pack
Reg. Nr.
Reg. Type
Reg. Date
Reg. Valid
Revocation
Company
1 bottle 120 dawek
1 bottle 30 dawek
22738
22738
MRP
MRP
08-10-2020
08-10-2020
20 tabs blister
20 tabs w fiolce
01713
01713
NP
NP
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Romania (2)
X
Product
Pack
Market
Pres.
Dosage
ATC
Company
1 flac. PEID, cu capacitatea de 20 ml, p
1 flac. PEID, cu capacitatea de 20 ml, p
-
-
P6L
P6L
-
R01AD11
1 tube x 15 g cream
-
PRF
-
D07XB02
Product
Pack
Reg. Nr.
Reg. Type
Reg. Date
Reg. Valid
Revocation
Company
1 flac. PEID, cu capacitatea de 20 ml, p
1 flac. PEID, cu capacitatea de 20 ml, p
-
-
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Slovenia (10)
X
Product
Pack
Market
Pres.
Dosage
ATC
Company
50 2 mg
-
Rx
oral
H02AB08
50 8 mg
-
Rx
oral
H02AB08
stekleničko 50 tabs
-
Rx
oral
H02AB08
5 amp 1 ml suspenzije
N
Rx
im/intraarticular
H02AB08
10 amp 1ml suspenzije
-
-
H02AB08
vsebnikom pršilno črpalko odmerjenim odm
-
Rx
nasal
R01AD11
vial blister ( 1x1 viala 1 ml suspenzije
-
-
S01BA05
1 vial 1 ml suspenzije
N
-
S01BA05
10 amuplami 1 ml suspenzije
N
Rx
intraarticular
H02AB08
Product
Pack
Reg. Nr.
Reg. Type
Reg. Date
Reg. Valid
Revocation
Company
50 2 mg
-
50 8 mg
-
stekleničko 50 tabs
5363-I-2267/11
NP
13-12-2011
5 amp 1 ml suspenzije
5363-I-97/09
NP
13-01-2009
10 amp 1 ml suspenzije
/
-
16-07-2010
16-07-2011
10 amp 1ml suspenzije
/
-
05-02-2014
05-02-2015
vsebnikom pršilno črpalko odmerjenim odm
10123-320/2016-5
MRP
23-05-2017
vial blister ( 1x1 viala 1 ml suspenzije
842-115/2018
-
16-03-2018
16-03-2019
1 vial 1 ml suspenzije
842-120/2019
-
15-03-2019
15-03-2020
10 amuplami 1 ml suspenzije
1011-12/2018-9
DCP
08-11-2018
Product
Pack
Ex-fact
Wholesale
Net retail
Gr. retail
Company
stekleničko 50 tabs
5 amp 1 ml suspenzije
13,5
vsebnikom pršilno črpalko odmerjenim odm
vial blister ( 1x1 viala 1 ml suspenzije
70,01
1 vial 1 ml suspenzije
153,06
10 amuplami 1 ml suspenzije
61,32
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Spain (4)
X
Product
Pack
Market
Pres.
Dosage
ATC
Company
10 amp of 1 ml
Y
Rx
intraarticular
H02AB08
1 tube of 30 g
Y
Rx
cut
D07XB02
1 envase pulverizador of 120 dosis
Y
Rx
nasal
R01AD11
1 amp of 1 ml
5 amp of 1 ml
Y
Y
Rx
Rx
VÍA INTRAARTICULAR, VÍA INTRAMUSCULAR, VÍA INTRASINOVIAL
H02AB08
Product
Pack
Reg. Nr.
Reg. Type
Reg. Date
Reg. Valid
Revocation
Company
10 amp of 1 ml
78545
20-03-2014
1 tube of 30 g
50543
01-03-1973
1 envase pulverizador of 120 dosis
61970
01-07-1998
1 amp of 1 ml
5 amp of 1 ml
44901
44901
01-09-1967
01-09-1967
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Sweden (14)
X
Product
Pack
Reg. Nr.
Reg. Type
Reg. Date
Reg. Valid
Revocation
Company
Nationell decentral eller ömsesidig
17-05-1995
15-05-2008
Nationell decentral eller ömsesidig
26-09-1960
31-10-2009
Nationell decentral eller ömsesidig
02-11-1966
31-01-2009
Nationell decentral eller ömsesidig
25-10-1963
30-04-2009
Nationell decentral eller ömsesidig
11-09-1981
Nationell decentral eller ömsesidig
19-04-1968
Nationell decentral eller ömsesidig
02-09-1965
31-10-2008
PI
20-09-2017
31-12-2019
Nationell decentral eller ömsesidig
09-05-1980
PI
PI
28-10-2015
28-10-2015
Nationell decentral eller ömsesidig
19-12-1997
Nationell decentral eller ömsesidig
05-10-2016
Nationell decentral eller ömsesidig
20-01-2012
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 (19)
X
Product
Pack
Reg. Nr.
Reg. Type
Reg. Date
Reg. Valid
Revocation
Company
24206 1
Hauptzulassung
07-01-1959
36566 2
36566 2
Hauptzulassung
Hauptzulassung
13-07-1972
13-07-1972
22-02-2024
22-02-2024
26177 1
26177 1
Hauptzulassung
Hauptzulassung
14-12-1959
14-12-1959
26177 2
Hauptzulassung
14-12-1959
32990 2
Hauptzulassung
12-07-1967
32990 1
32990 1
32990 1
Hauptzulassung
Hauptzulassung
Hauptzulassung
12-07-1967
12-07-1967
12-07-1967
35039 1
Hauptzulassung
16-04-1970
16-12-2023
38774 8
Hauptzulassung
02-09-1975
38774 9
Hauptzulassung
02-09-1975
38774 10
38774 10
Hauptzulassung
Hauptzulassung
02-09-1975
02-09-1975
29621 1
Hauptzulassung
18-03-1963
04-10-2022
53892 1
Hauptzulassung
29-11-1996
05-09-2020
61855 1
Hauptzulassung
30-09-2010
29-09-2020
41174 1
41174 1
Hauptzulassung
Hauptzulassung
23-12-1977
23-12-1977
24-10-2022
24-10-2022
41174 3
41174 3
Hauptzulassung
Hauptzulassung
23-12-1977
23-12-1977
24-10-2022
24-10-2022
41174 2
41174 2
Hauptzulassung
Hauptzulassung
23-12-1977
23-12-1977
24-10-2022
24-10-2022
41174 4
41174 4
Hauptzulassung
Hauptzulassung
23-12-1977
23-12-1977
24-10-2022
24-10-2022
62962 1
62962 1
Hauptzulassung
Hauptzulassung
04-09-2014
04-09-2014
61565 1
Hauptzulassung
20-10-2011
19-10-2021
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