All the information on this site is from our Global Pharmaceutical Database.
pethidine
N02AB02
North America
Canada (2)
X
United States (61)Product
Pack
Market
Pres.
Dosage
ATC
Company
Product
Pack
Reg. Nr.
Reg. Type
Reg. Date
Reg. Valid
Revocation
Company
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X
Product
Pack
Market
Pres.
Dosage
ATC
Company
N
INJECTION
N02AB02
Product
Pack
Reg. Nr.
Reg. Type
Reg. Date
Reg. Valid
Revocation
Company
89788/1
89787/1
89786/1
89787/1
89786/1
ANDA
ANDA
ANDA
ANDA
ANDA
31-03-1989
31-03-1989
31-03-1989
31-03-1989
31-03-1989
89784/1
89783/1
89782/1
89783/1
89782/1
ANDA
ANDA
ANDA
ANDA
ANDA
31-03-1989
31-03-1989
31-03-1989
31-03-1989
31-03-1989
81309/1
ANDA
30-08-1993
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Europe
Austria (1)
X
Belgium (2)Product
Pack
Market
Pres.
Dosage
ATC
Company
Product
Pack
Reg. Nr.
Reg. Type
Reg. Date
Reg. Valid
Revocation
Company
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X
Croatia (0)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
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No result.
Czechia (1)
X
Denmark (2)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.
X
Hungary (1)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.
X
Iceland (1)Product
Pack
Market
Pres.
Dosage
ATC
Company
Product
Pack
Reg. Nr.
Reg. Type
Reg. Date
Reg. Valid
Revocation
Company
25x2ml amp
5x2ml amp
5x2ml amp
OGYI-T-12707/02
OGYI-T-12707/01
OGYI-T-12707/01
01-01-1939
01-01-1939
01-01-1939
Product
Pack
Ex-fact
Wholesale
Net retail
Gr. retail
Company
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X
Ireland (5)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.
X
Lithuania (1)Product
Pack
Market
Pres.
Dosage
ATC
Company
Product
Pack
Reg. Nr.
Reg. Type
Reg. Date
Reg. Valid
Revocation
Company
PA0361/008/003
13-12-1996
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X
Malta (10)Product
Pack
Market
Pres.
Dosage
ATC
Company
Product
Pack
Reg. Nr.
Reg. Type
Reg. Date
Reg. Valid
Revocation
Company
1 ml N10 amp
2 ml N10 amp
2 ml N10 amp
LT/1/97/1719/001
LT/1/97/1719/002
LT/1/97/1719/002
NP
NP
NP
06-06-1997
06-06-1997
06-06-1997
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X
Poland (1)Product
Pack
Market
Pres.
Dosage
ATC
Company
Product
Pack
Reg. Nr.
Reg. Type
Reg. Date
Reg. Valid
Revocation
Company
PI565/43401A
02-04-2019
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X
Romania (1)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.
X
Slovenia (11)Product
Pack
Market
Pres.
Dosage
ATC
Company
x 10 fiole din sticla prevazute cu inel
x 5 fiole din sticla prevazute cu inel d
x 5 fiole din sticla prevazute cu inel d
-
-
-
PS
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
x 5 fiole din sticla prevazute cu inel d
-
-
-
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X
Spain (2)Product
Pack
Market
Pres.
Dosage
ATC
Company
Product
Pack
Reg. Nr.
Reg. Type
Reg. Date
Reg. Valid
Revocation
Company
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
Product
Pack
Ex-fact
Wholesale
Net retail
Gr. retail
Company
ampule 25x100mg/2ml
5 amp 2 ml sol
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X
Sweden (1)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
1 amp of 2 ml
10 amp of 1 ml
10 amp of 2 ml
Y
Y
Y
Y
Y
Y
Y
Rx
Rx
Rx
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
1 amp of 2 ml
10 amp of 1 ml
10 amp of 2 ml
-
-
Y
Y
-
Y
Y
Rx
Rx
Rx
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
1 amp of 2 ml
10 amp of 1 ml
10 amp of 2 ml
24245
24245
24245
24245
24245
24245
24245
01-07-1955
01-07-1955
01-07-1955
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
1 amp of 2 ml
10 amp of 1 ml
10 amp of 2 ml
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72848
13-10-2010
13-10-2010
13-10-2010
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.
X
Switzerland (6)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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X
Product
Pack
Market
Pres.
Dosage
ATC
Company
Product
Pack
Reg. Nr.
Reg. Type
Reg. Date
Reg. Valid
Revocation
Company
52109 1
52109 1
52109 1
Hauptzulassung
Hauptzulassung
Hauptzulassung
16-02-1994
16-02-1994
16-02-1994
22-02-2024
22-02-2024
22-02-2024
53572 1
53572 1
53572 1
Hauptzulassung
Hauptzulassung
Hauptzulassung
14-12-1998
14-12-1998
14-12-1998
22-02-2024
22-02-2024
22-02-2024
53572 2
53572 2
53572 2
Hauptzulassung
Hauptzulassung
Hauptzulassung
14-12-1998
14-12-1998
14-12-1998
22-02-2024
22-02-2024
22-02-2024
13369 1
13369 1
13369 1
Hauptzulassung
Hauptzulassung
Hauptzulassung
22-01-1947
22-01-1947
22-01-1947
20-12-2022
20-12-2022
20-12-2022
13369 2
13369 2
13369 2
Hauptzulassung
Hauptzulassung
Hauptzulassung
22-01-1947
22-01-1947
22-01-1947
20-12-2022
20-12-2022
20-12-2022
22672 1
22672 1
22672 1
22672 1
22672 1
Hauptzulassung
Hauptzulassung
Hauptzulassung
Hauptzulassung
Hauptzulassung
09-08-1956
09-08-1956
09-08-1956
09-08-1956
09-08-1956
27-05-2024
27-05-2024
27-05-2024
27-05-2024
27-05-2024
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.
