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

pethidine

North America

Canada (2)
X
Product
Pack
Market
Pres.
Dosage
ATC
Company
Narcotic (CDSA I)
oral
N02AB02
Narcotic (CDSA I)
iv/im/subcut
N02AB02
Product
Pack
Reg. Nr.
Reg. Type
Reg. Date
Reg. Valid
Revocation
Company
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United States (61)
X
Product
Pack
Market
Pres.
Dosage
ATC
Company
Y
Rx
INJECTION
N02AB02
Y
Rx
INJECTION
N02AB02
Y
Rx
INJECTION
N02AB02
Y
Rx
INJECTION
N02AB02
Product
Pack
Reg. Nr.
Reg. Type
Reg. Date
Reg. Valid
Revocation
Company
21171/4
NDA
01-01-1982
21171/1
NDA
01-01-1982
21171/2
NDA
01-01-1982
21171/3
NDA
01-01-1982
88640/1
ANDA
19-09-1984
40110/2
ANDA
12-03-1997
80448/2
40446/2
ANDA
ANDA
01-01-1982
08-08-2002
89788/1
89787/1
89786/1
ANDA
ANDA
ANDA
31-03-1989
31-03-1989
31-03-1989
80445/4
80455/10
ANDA
ANDA
01-01-1982
01-01-1982
80445/1
80455/7
ANDA
ANDA
01-01-1982
01-01-1982
88639/1
ANDA
02-07-1984
40110/1
ANDA
12-03-1997
40352/1
ANDA
13-06-2000
80448/1
40446/1
ANDA
ANDA
01-01-1982
08-08-2002
40186/1
ANDA
30-06-1997
80454/1
ANDA
01-01-1982
80387/1
80385/1
ANDA
ANDA
01-01-1982
01-01-1982
89784/1
89783/1
89782/1
ANDA
ANDA
ANDA
31-03-1989
31-03-1989
31-03-1989
80445/2
80455/8
ANDA
ANDA
01-01-1982
01-01-1982
80445/3
80455/9
ANDA
ANDA
01-01-1982
01-01-1982
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Europe

Austria (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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Belgium (2)
X
Product
Pack
Market
Pres.
Dosage
ATC
Company
2 mL
2 mL
2 mL
N
Y
Y


iv/im/subcut
N02AB02
1 mL
-
iv/im/subcut
N02AB02
Product
Pack
Reg. Nr.
Reg. Type
Reg. Date
Reg. Valid
Revocation
Company
2 mL
2 mL
2 mL
BE489653
BE489653
BE489653
-
-
-
Product
Pack
Ex-fact
Wholesale
Net retail
Gr. retail
Company
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Croatia (0)
No result.
Czechia (1)
X
Product
Pack
Market
Pres.
Dosage
ATC
Company
50MG/ML 10X1ML
50MG/ML 10X2ML
Y
Y
iv/im/subcut
N02AB02
Product
Pack
Reg. Nr.
Reg. Type
Reg. Date
Reg. Valid
Revocation
Company
50MG/ML 10X1ML
50MG/ML 10X2ML
65/ 764/92-S/C
65/ 764/92-S/C
NP
NP
Product
Pack
Ex-fact
Wholesale
Net retail
Gr. retail
Company
50MG/ML 10X1ML
50MG/ML 10X2ML
69,2
88,45
104,28
133,29
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Denmark (2)
X
Product
Pack
Market
Pres.
Dosage
ATC
Company
Product
Pack
Reg. Nr.
Reg. Type
Reg. Date
Reg. Valid
Revocation
Company
28100743376
NP
01-08-1977
28100743476
NP
01-08-1977
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Hungary (1)
X
Product
Pack
Market
Pres.
Dosage
ATC
Company
25x2ml amp
5x2ml amp
Y
Y
Rx
Rx
parenteral
N02AB02
Product
Pack
Reg. Nr.
Reg. Type
Reg. Date
Reg. Valid
Revocation
Company
25x2ml amp
5x2ml amp
OGYI-T-12707/02
OGYI-T-12707/01
01-01-1939
01-01-1939
Product
Pack
Ex-fact
Wholesale
Net retail
Gr. retail
Company
25x2ml amp
5x2ml amp
0
0
0
0
0
0
0
0
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Iceland (1)
X
Product
Pack
Market
Pres.
Dosage
ATC
Company
Product
Pack
Reg. Nr.
Reg. Type
Reg. Date
Reg. Valid
Revocation
Company
Product
Pack
Ex-fact
Wholesale
Net retail
Gr. retail
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 (5)
X
Product
Pack
Reg. Nr.
Reg. Type
Reg. Date
Reg. Valid
Revocation
Company
PA0361/008/001
13-12-1996
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Lithuania (1)
X
Product
Pack
Market
Pres.
Dosage
ATC
Company
1 ml N10 amp
2 ml N10 amp
Rx
Rx
iv/im/subcut
N02AB02
Product
Pack
Reg. Nr.
Reg. Type
Reg. Date
Reg. Valid
Revocation
Company
1 ml N10 amp
2 ml N10 amp
LT/1/97/1719/001
LT/1/97/1719/002
NP
NP
06-06-1997
06-06-1997
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Malta (10)
X
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Poland (1)
X
Product
Pack
Market
Pres.
Dosage
ATC
Company
10 amp 1 ml
10 amp 2 ml
Rpw
Rpw
-
N02AB02
Product
Pack
Reg. Nr.
Reg. Type
Reg. Date
Reg. Valid
Revocation
Company
10 amp 1 ml
10 amp 2 ml
03546
03546
NP
NP
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Romania (1)
X
Product
Pack
Market
Pres.
Dosage
ATC
Company
x 10 fiole din sticla prevazute cu inel
x 5 fiole din sticla prevazute cu inel d
-
-
PS
PS
-
N02AB02
Product
Pack
Reg. Nr.
Reg. Type
Reg. Date
Reg. Valid
Revocation
Company
x 10 fiole din sticla prevazute cu inel
x 5 fiole din sticla prevazute cu inel d
-
-
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Slovenia (11)
X
Product
Pack
Market
Pres.
Dosage
ATC
Company
5 amp 2 ml sol
N
-
N02AB02
ampule 25x100mg/2ml
-
Rx
parenteral
N02AB02
5 amp 2 ml sol
-
Rx
parenteral
N02AB02
5 ampul 2 ml sol
N
-
N02AB02
5 amp 2 ml sol
-
-
N02AB02
10 amp 2 ml sol
-
-
N02AB02
10 amp 2 ml sol
N
-
N02AB02
Product
Pack
Reg. Nr.
Reg. Type
Reg. Date
Reg. Valid
Revocation
Company
5 amp 2 ml sol
842-336/2019
-
26-08-2019
26-08-2020
ampule 25x100mg/2ml
-
5 ampul 2 ml sol
/
-
22-01-2016
21-01-2017
5 amp 2 ml sol
/
-
04-01-2016
04-01-2017
10 amp 2 ml sol
842-117/2019
-
11-03-2019
11-03-2020
10 amp 2 ml sol
842-214/2019
-
16-05-2019
16-05-2020
10 amp 2 ml
842-306/2016
-
16-01-2017
16-01-2018
10 amp 2 ml sol
842-227/2017
-
17-10-2017
17-10-2018
17-04-2020
10 amp 2 ml sol
842-340/2018
-
04-10-2018
04-10-2019
10 amp 2 ml sol
842-373/2018
-
25-10-2018
25-10-2019
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Spain (2)
X
Product
Pack
Market
Pres.
Dosage
ATC
Company
1 amp of 1 ml
1 amp of 2 ml
10 amp of 1 ml
10 amp of 2 ml
Y
Y
Y
Y
Rx
Rx
Rx
Rx
iv/im/subcut
N02AB02
1 amp of 1 ml
1 amp of 2 ml
10 amp of 1 ml
10 amp of 2 ml
-
-
Y
Y
Rx
Rx
Rx
Rx
VÍA SUBCUTÁNEA, VÍA INTRAMUSCULAR, VÍA INTRAVENOSA
N02AB02
Product
Pack
Reg. Nr.
Reg. Type
Reg. Date
Reg. Valid
Revocation
Company
1 amp of 1 ml
1 amp of 2 ml
10 amp of 1 ml
10 amp of 2 ml
24245
24245
24245
24245
01-07-1955
01-07-1955
01-07-1955
01-07-1955
1 amp of 1 ml
1 amp of 2 ml
10 amp of 1 ml
10 amp of 2 ml
72848
72848
72848
72848
13-10-2010
13-10-2010
13-10-2010
13-10-2010
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.

Sweden (1)
X
Product
Pack
Market
Pres.
Dosage
ATC
Company
Product
Pack
Reg. Nr.
Reg. Type
Reg. Date
Reg. Valid
Revocation
Company
Nationell decentral eller ömsesidig
06-12-1974
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Switzerland (6)
X
Product
Pack
Reg. Nr.
Reg. Type
Reg. Date
Reg. Valid
Revocation
Company
52109 1
52109 1
Hauptzulassung
Hauptzulassung
16-02-1994
16-02-1994
22-02-2024
22-02-2024
53572 1
53572 1
Hauptzulassung
Hauptzulassung
14-12-1998
14-12-1998
22-02-2024
22-02-2024
53572 2
53572 2
Hauptzulassung
Hauptzulassung
14-12-1998
14-12-1998
22-02-2024
22-02-2024
13369 1
13369 1
Hauptzulassung
Hauptzulassung
22-01-1947
22-01-1947
20-12-2022
20-12-2022
13369 2
13369 2
Hauptzulassung
Hauptzulassung
22-01-1947
22-01-1947
20-12-2022
20-12-2022
22672 1
22672 1
22672 1
Hauptzulassung
Hauptzulassung
Hauptzulassung
09-08-1956
09-08-1956
09-08-1956
27-05-2024
27-05-2024
27-05-2024
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