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

sufentanil

North America

Canada (2)
X
Product
Pack
Market
Pres.
Dosage
ATC
Company
Narcotic (CDSA I)
iv/epid
N01AH03
Narcotic (CDSA I)
iv/epid
N01AH03
Product
Pack
Reg. Nr.
Reg. Type
Reg. Date
Reg. Valid
Revocation
Company
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United States (5)
X
Product
Pack
Market
Pres.
Dosage
ATC
Company
Product
Pack
Reg. Nr.
Reg. Type
Reg. Date
Reg. Valid
Revocation
Company
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Europe

Austria (8)
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.

Belgium (6)
X
Product
Pack
Market
Pres.
Dosage
ATC
Company
10 mL
10 mL
2 mL
2 mL
Y
-
Y
-



iv/epid
N01AH03
5 mL
5 mL
Y
-

iv/epid
N01AH03
10 mL
10 mL
2 mL
2 mL
-
Y
Y
-



iv/epid
N01AH03
5 mL
5 mL
5 mL
Y
N
-


iv/epid
N01AH03
40x
40x
40x
-
Y
-


sublingual
N01AH03
Product
Pack
Reg. Nr.
Reg. Type
Reg. Date
Reg. Valid
Revocation
Company
1x
1x
EU/1/18/1284/002
EU/1/18/1284/001
CP
CP
10 mL
10 mL
2 mL
2 mL
BE111447
BE111447
BE111431
BE111431
-
-
-
-
5 mL
5 mL
BE111456
BE111456
-
-
10 mL
10 mL
2 mL
2 mL
BE308183
BE308183
BE288547
BE288547
-
-
-
-
5 mL
5 mL
5 mL
BE288556
BE288556
BE288556
-
-
-
40x
40x
40x
EU/1/15/1042/003
EU/1/15/1042/003
EU/1/15/1042/002
CP
CP
CP
Product
Pack
Ex-fact
Wholesale
Net retail
Gr. retail
Company
10 mL
10 mL
2 mL
2 mL
4,81
1,19
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Croatia (5)
X
Product
Pack
Market
Pres.
Dosage
ATC
Company
-
Rx
-
N01AH03
10 amp 10 ml otopina u ulošku folijom
5 amp 10 ml otopina u ulošku folijom
N
N
Rx
Rx
-
N01AH03
10 amp 5 ml otopina u ulošku folijom
5 amp 5 ml otopina u ulošku folijom
N
N
Rx
Rx
-
N01AH03
-
Rx
-
N01AH03
Product
Pack
Reg. Nr.
Reg. Type
Reg. Date
Reg. Valid
Revocation
Company
10 amp 10 ml otopina u ulošku folijom
5 amp 10 ml otopina u ulošku folijom
HR-H-546847501-02
HR-H-546847501-01
07-01-2019
07-01-2019
07-01-2024
07-01-2024
10 amp 5 ml otopina u ulošku folijom
5 amp 5 ml otopina u ulošku folijom
HR-H-353313890-02
HR-H-353313890-01
07-01-2019
07-01-2019
07-01-2024
07-01-2024
10 amp 10 ml otopina
HR-H-677795227-01
29-11-2019
29-11-2024
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Czechia (11)
X
Product
Pack
Market
Pres.
Dosage
ATC
Company
30MCG 10X1
30MCG 5X1
N
N
sublingual
N01AH03
50MCG/ML 10X5ML
50MCG/ML 5X5ML
N
N
iv/epid
N01AH03
5MCG/ML 10X10ML
5MCG/ML 5X10ML
N
N
iv/epid
N01AH03
5MCG/ML 5X2ML
Y
iv/epid
N01AH03
5MCG/ML 5X2ML
N
iv/epid
N01AH03
5MCG/ML 5X2ML
N
iv/epid
N01AH03
50MCG/ML 5X1ML
50MCG/ML 5X5ML
Y
Y
iv/epid
N01AH03
50MCG/ML 5X1ML
50MCG/ML 5X5ML
N
N
iv/epid
N01AH03
50MCG/ML 5X1ML
50MCG/ML 5X5ML
Y
N
iv/epid
N01AH03
50MCG/ML 10X20ML
50MCG/ML 10X20ML
50MCG/ML 10X5ML
50MCG/ML 10X5ML
50MCG/ML 20X20ML
50MCG/ML 20X20ML
50MCG/ML 20X5ML
50MCG/ML 20X5ML
50MCG/ML 5X20ML
50MCG/ML 5X20ML
50MCG/ML 5X5ML
50MCG/ML 5X5ML
N
N
N
N
N
N
N
N
N
N
Y
Y
iv/epid
N01AH03
5MCG/ML 10X10ML
5MCG/ML 10X10ML
5MCG/ML 20X10ML
5MCG/ML 20X10ML
5MCG/ML 5X10ML
5MCG/ML 5X10ML
5MCG/ML 5X2ML
5MCG/ML 5X2ML
N
N
N
N
N
Y
Y
Y
iv/epid
N01AH03
15MCG 100(5X20)X40 TBL
15MCG 10X40 TBL
15MCG 1X40 TBL
15MCG 20X40 TBL
15MCG 40(2X20)X40 TBL
15MCG 60(3X20)X40 TBL
N
N
N
N
N
N
sublingual
N01AH03
Product
Pack
Reg. Nr.
Reg. Type
Reg. Date
Reg. Valid
Revocation
Company
30MCG 10X1
30MCG 5X1
EU/1/18/1284/002
EU/1/18/1284/001
CP
CP
50MCG/ML 10X5ML
50MCG/ML 5X5ML
65/ 460/17-C
65/ 460/17-C
MRP/DCP
MRP/DCP
5MCG/ML 10X10ML
5MCG/ML 5X10ML
65/ 459/17-C
65/ 459/17-C
MRP/DCP
MRP/DCP
5MCG/ML 5X2ML
65/ 309/91-A/C
NP
5MCG/ML 5X2ML
65/ 309/91-A/C
NP
5MCG/ML 5X2ML
65/ 309/91-A/C
NP
50MCG/ML 5X1ML
50MCG/ML 5X5ML
65/ 309/91-B/C
65/ 309/91-B/C
NP
NP
50MCG/ML 5X1ML
50MCG/ML 5X5ML
65/ 309/91-B/C
65/ 309/91-B/C
NP
NP
50MCG/ML 5X1ML
50MCG/ML 5X5ML
65/ 309/91-B/C
65/ 309/91-B/C
NP
NP
50MCG/ML 10X20ML
50MCG/ML 10X20ML
50MCG/ML 10X5ML
50MCG/ML 10X5ML
50MCG/ML 20X20ML
50MCG/ML 20X20ML
50MCG/ML 20X5ML
50MCG/ML 20X5ML
50MCG/ML 5X20ML
50MCG/ML 5X20ML
50MCG/ML 5X5ML
50MCG/ML 5X5ML
65/ 044/03-C
65/ 044/03-C
65/ 044/03-C
65/ 044/03-C
65/ 044/03-C
65/ 044/03-C
65/ 044/03-C
65/ 044/03-C
65/ 044/03-C
65/ 044/03-C
65/ 044/03-C
65/ 044/03-C
NP
NP
NP
NP
NP
NP
NP
NP
NP
NP
NP
NP
5MCG/ML 10X10ML
5MCG/ML 10X10ML
5MCG/ML 20X10ML
5MCG/ML 20X10ML
5MCG/ML 5X10ML
5MCG/ML 5X10ML
5MCG/ML 5X2ML
5MCG/ML 5X2ML
65/ 043/03-C
65/ 043/03-C
65/ 043/03-C
65/ 043/03-C
65/ 043/03-C
65/ 043/03-C
65/ 043/03-C
65/ 043/03-C
NP
NP
NP
NP
NP
NP
NP
NP
15MCG 100(5X20)X40 TBL
15MCG 10X40 TBL
15MCG 1X40 TBL
15MCG 20X40 TBL
15MCG 40(2X20)X40 TBL
15MCG 60(3X20)X40 TBL
EU/1/15/1042/006
EU/1/15/1042/002
EU/1/15/1042/001
EU/1/15/1042/003
EU/1/15/1042/004
EU/1/15/1042/005
CP
CP
CP
CP
CP
CP
Product
Pack
Ex-fact
Wholesale
Net retail
Gr. retail
Company
30MCG 10X1
30MCG 5X1
0
0
50MCG/ML 10X5ML
50MCG/ML 5X5ML
0
610,87
864,65
5MCG/ML 10X10ML
5MCG/ML 5X10ML
0
131,7
198,47
5MCG/ML 5X2ML
72,17
108,76
5MCG/ML 5X2ML
72,17
108,76
5MCG/ML 5X2ML
72,17
108,76
50MCG/ML 5X1ML
50MCG/ML 5X5ML
128,07
610,87
193
864,65
50MCG/ML 5X1ML
50MCG/ML 5X5ML
128,07
610,87
193
864,65
50MCG/ML 5X1ML
50MCG/ML 5X5ML
128,07
610,87
193
864,65
50MCG/ML 10X20ML
50MCG/ML 10X20ML
50MCG/ML 10X5ML
50MCG/ML 10X5ML
50MCG/ML 20X20ML
50MCG/ML 20X20ML
50MCG/ML 20X5ML
50MCG/ML 20X5ML
50MCG/ML 5X20ML
50MCG/ML 5X20ML
50MCG/ML 5X5ML
50MCG/ML 5X5ML
0
0
0
0
0
0
0
0
0
0
610,87
610,87


864,65
864,65
5MCG/ML 10X10ML
5MCG/ML 10X10ML
5MCG/ML 20X10ML
5MCG/ML 20X10ML
5MCG/ML 5X10ML
5MCG/ML 5X10ML
5MCG/ML 5X2ML
5MCG/ML 5X2ML
0
0
0
0
131,7
131,7
78,9
78,9
198,47
198,47
118,9
118,9
15MCG 100(5X20)X40 TBL
15MCG 10X40 TBL
15MCG 1X40 TBL
15MCG 20X40 TBL
15MCG 40(2X20)X40 TBL
15MCG 60(3X20)X40 TBL
0
0
0
0
0
0
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Denmark (9)
X
Product
Pack
Reg. Nr.
Reg. Type
Reg. Date
Reg. Valid
Revocation
Company
28101389489
NP
30-01-1991
28101389589
NP
30-01-1991
28105484714
CP
18-09-2015
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Hungary (4)
X
Product
Pack
Market
Pres.
Dosage
ATC
Company
10x1 single-dose applikátorokban
5x1 single-dose applikátorokban
N
N
Rx
Rx
oromucosal
N01AH03
5x10ml amp
N
Rx
parenteral
N01AH03
5x20ml amp
5x5ml amp
N
N
Rx
Rx
parenteral
N01AH03
1600x cartridge
2400x cartridge
4000x cartridge
400x cartridge
40x cartridge
800x cartridge
N
N
N
N
N
N
Rx
Rx
Rx
Rx
Rx
Rx
oromucosal
N01AH03
Product
Pack
Reg. Nr.
Reg. Type
Reg. Date
Reg. Valid
Revocation
Company
10x1 single-dose applikátorokban
5x1 single-dose applikátorokban
EU/1/18/1284/002
EU/1/18/1284/001
25-06-2018
25-06-2018
5x10ml amp
OGYI-T-08710/01
5x20ml amp
5x5ml amp
OGYI-T-08710/03
OGYI-T-08710/02
1600x cartridge
2400x cartridge
4000x cartridge
400x cartridge
40x cartridge
800x cartridge
EU/1/15/1042/004
EU/1/15/1042/005
EU/1/15/1042/006
EU/1/15/1042/002
EU/1/15/1042/001
EU/1/15/1042/003
18-09-2015
18-09-2015
18-09-2015
18-09-2015
18-09-2015
18-09-2015
Product
Pack
Ex-fact
Wholesale
Net retail
Gr. retail
Company
10x1 single-dose applikátorokban
5x1 single-dose applikátorokban
0
0
0
0
0
0
0
0
5x20ml amp
5x5ml amp
16500
5000
17226
5220
18216
6160
19127
6468
1600x cartridge
2400x cartridge
4000x cartridge
400x cartridge
40x cartridge
800x cartridge
0
0
0
0
0
0
0
0
0
0
0
0
0
0
0
0
0
0
0
0
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
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Ireland (2)
X
Product
Pack
Market
Pres.
Dosage
ATC
Company
-
Rx
sublingual
N01AH03
Product
Pack
Reg. Nr.
Reg. Type
Reg. Date
Reg. Valid
Revocation
Company
EU/1/18/1284/001-002
25-06-2018
EU/1/15/1042/001-006
18-09-2015
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Lithuania (4)
X
Product
Pack
Market
Pres.
Dosage
ATC
Company
N10x1 vienadozis aplikatorius
N5x1 vienadozis aplikatorius
Rx
Rx
sublingual
N01AH03
10 ml N10 amp
10 ml N5 amp
Rx
Rx
iv/epid
N01AH03
5 ml N10 amp
5 ml N5 amp
Rx
Rx
leisti į epidurinę ertmę;leisti į veną
N01AH03
N1600 (2x20x40) (sudėtinė) užtaisas
N2400 (3x20x40) (sudėtinė) užtaisas
N40 (1x40) užtaisas
N400 (10x40) užtaisas
N4000 (5x20x40) (sudėtinė) užtaisas
N800 (20x40) užtaisas
Rx
Rx
Rx
Rx
Rx
Rx
sublingual
N01AH03
Product
Pack
Reg. Nr.
Reg. Type
Reg. Date
Reg. Valid
Revocation
Company
N10x1 vienadozis aplikatorius
N5x1 vienadozis aplikatorius
EU/1/18/1284/002
EU/1/18/1284/001
CP
CP
25-06-2018
25-06-2018
10 ml N10 amp
10 ml N5 amp
LT/1/18/4321/002
LT/1/18/4321/001
DCP
DCP
28-12-2018
28-12-2018
5 ml N10 amp
5 ml N5 amp
LT/1/18/4322/002
LT/1/18/4322/001
DCP
DCP
28-12-2018
28-12-2018
N1600 (2x20x40) (sudėtinė) užtaisas
N2400 (3x20x40) (sudėtinė) užtaisas
N40 (1x40) užtaisas
N400 (10x40) užtaisas
N4000 (5x20x40) (sudėtinė) užtaisas
N800 (20x40) užtaisas
EU/1/15/1042/004
EU/1/15/1042/005
EU/1/15/1042/001
EU/1/15/1042/002
EU/1/15/1042/006
EU/1/15/1042/003
CP
CP
CP
CP
CP
CP
18-09-2015
18-09-2015
18-09-2015
18-09-2015
18-09-2015
18-09-2015
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Malta (3)
X
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 (4)
X
Product
Pack
Market
Pres.
Dosage
ATC
Company
5 amp 10 ml
5 amp 2 ml
Lz
Lz
-
N01AH03
1600 tabs
2400 tabs
40 tabs
400 tabs
4000 tabs
800 tabs
-
N01AH03
Product
Pack
Reg. Nr.
Reg. Type
Reg. Date
Reg. Valid
Revocation
Company
5 amp 10 ml
5 amp 2 ml
10245
10245
NP
NP
1600 tabs
2400 tabs
40 tabs
400 tabs
4000 tabs
800 tabs
CP
CP
CP
CP
CP
CP
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Romania (2)
X
Product
Pack
Market
Pres.
Dosage
ATC
Company
1 tava din PVC x 10 fiole x 5 ml sol. in
1 tava din PVC x 5 fiole x 5 ml sol. inj
-
-
PR
PR
-
N01AH03
1 tava din PVC x 10 fiole x 5 ml sol. in
1 tava din PVC x 5 fiole x 5 ml sol. inj
-
-
PR
PR
-
N01AH03
Product
Pack
Reg. Nr.
Reg. Type
Reg. Date
Reg. Valid
Revocation
Company
1 tava din PVC x 10 fiole x 5 ml sol. in
1 tava din PVC x 5 fiole x 5 ml sol. inj
-
-
1 tava din PVC x 10 fiole x 5 ml sol. in
1 tava din PVC x 5 fiole x 5 ml sol. inj
-
-
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Slovenia (7)
X
Product
Pack
Market
Pres.
Dosage
ATC
Company
5 amp 2 ml sol (0,005 mg/ml)
-
Rx
parenteral
N01AH03
5 amp 5 ml sol (0,05 mg/ml)
-
Rx
parenteral
N01AH03
10 amp 10 ml sol
-
-
N01AH03
5 amp 10 ml sol
N
Rx
iv
N01AH03
5 amp 20 ml sol
5 amp 5 ml sol
N
N
Rx
Rx
iv
N01AH03
10 amp 10 ml sol
5 amp 10 ml sol
-
-

-
N01AH03
Product
Pack
Reg. Nr.
Reg. Type
Reg. Date
Reg. Valid
Revocation
Company
5 amp 2 ml sol (0,005 mg/ml)
-
5 amp 5 ml sol (0,05 mg/ml)
-
10 amp 10 ml sol
/
-
22-09-2014
22-09-2015
5 amp 10 ml sol
103-131/2014-2
NP
07-10-2014
07-10-2014
07-12-2014
5 amp 20 ml sol
5 amp 5 ml sol
103-131/2014-2
103-131/2014-2
NP
NP
07-10-2014
07-10-2014
07-10-2014
07-10-2014
07-12-2014
07-12-2014
5 amp 5 ml sol
/
-
20-05-2015
19-05-2016
10 amp 10 ml sol
5 amp 10 ml sol
/
841-101/2019
-
-
09-04-2020
04-09-2019
09-04-2021
04-09-2020
Product
Pack
Ex-fact
Wholesale
Net retail
Gr. retail
Company
5 amp 2 ml sol (0,005 mg/ml)
5 amp 5 ml sol (0,05 mg/ml)
10 amp 10 ml sol
5 amp 10 ml sol
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Spain (3)
X
Product
Pack
Market
Pres.
Dosage
ATC
Company
10 amp of 10 ml
10 amp of 2 ml
5 amp of 2 ml
-
Y
-
Rx
Rx
Rx
iv/epid
N01AH03
20 cartuchos con 40 tabs sublinguales ca
Y
Rx
sublingual
N01AH03
Product
Pack
Reg. Nr.
Reg. Type
Reg. Date
Reg. Valid
Revocation
Company
10 amp of 10 ml
10 amp of 2 ml
5 amp of 2 ml
70299
70299
70299
10-12-2008
10-12-2008
10-12-2008
20 cartuchos con 40 tabs sublinguales ca
1151042003
24-11-2015
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Sweden (4)
X
Product
Pack
Reg. Nr.
Reg. Type
Reg. Date
Reg. Valid
Revocation
Company
Nationell decentral eller ömsesidig
06-09-1991
Nationell decentral eller ömsesidig
06-09-1991
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Switzerland (4)
X
Product
Pack
Reg. Nr.
Reg. Type
Reg. Date
Reg. Valid
Revocation
Company
52413 1
52413 1
Hauptzulassung
Hauptzulassung
27-06-1994
27-06-1994
28-10-2023
28-10-2023
52413 2
52413 2
Hauptzulassung
Hauptzulassung
27-06-1994
27-06-1994
28-10-2023
28-10-2023
60133 2
Exportzulassung
19-10-2010
18-10-2020
60133 1
Exportzulassung
19-10-2010
18-10-2020
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.