pethidine
North America
Canada (1)
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
MEPERIDINE HYDROCHLORIDE PRESERVATIVE FREE 10MG/ML inj
N
INJECTION
N02AB02
Product
Pack
Reg. Nr.
Reg. Type
Reg. Date
Reg. Valid
Revocation
Company
MEPERIDINE HYDROCHLORIDE 100MG/ML inj
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
MEPERIDINE HYDROCHLORIDE 50MG/ML inj
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
MEPERIDINE HYDROCHLORIDE PRESERVATIVE FREE 10MG/ML inj
81309/1
ANDA
30-08-1993
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Europe
Austria (1)
X
Belgium (2)Product
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Product
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X
Bosnia and Herzegovina (0)Product
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Revocation
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Product
Pack
Ex-fact
Wholesale
Net retail
Gr. retail
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No result.
Croatia (0)
No result.
Czechia (1)
X
Denmark (2)Product
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Product
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Product
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Ex-fact
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X
Finland (0)Product
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Company
Product
Pack
Ex-fact
Wholesale
Net retail
Gr. retail
Company
PETIDIN DAK 100 MG supp
PETIDIN DAK 25 MG tabs
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No result.
Hungary (2)
X
Iceland (0)Product
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Product
Pack
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DOLARGAN sol for inj
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
01-02-2021
01-02-2021
01-02-2021
Product
Pack
Ex-fact
Wholesale
Net retail
Gr. retail
Company
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No result.
Ireland (2)
X
Lithuania (2)Product
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Market
Pres.
Dosage
ATC
Company
Product
Pack
Reg. Nr.
Reg. Type
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X
Malta (9)Product
Pack
Market
Pres.
Dosage
ATC
Company
Product
Pack
Reg. Nr.
Reg. Type
Reg. Date
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Revocation
Company
DOLOBLOK 50 MG/ML sol for inj
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
DOLSIN 50 MG/ML sol for inj
1 ml N10 amp
2 ml N10 amp
2 ml N10 amp
LT/L/21/1501/001
LT/L/21/1501/002
LT/L/21/1501/002
PI
PI
PI
29-03-2021
29-03-2021
29-03-2021
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X
Netherlands (1)Product
Pack
Market
Pres.
Dosage
ATC
Company
Product
Pack
Reg. Nr.
Reg. Type
Reg. Date
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Revocation
Company
PETHIDINE HYDROCHLORIDE 50MG/ML sol for inj
PI565/43401A
02-04-2019
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X
Norway (2)Product
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Product
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X
Poland (1)Product
Pack
Market
Pres.
Dosage
ATC
Company
PETHIDIN HCL 50 MG/ML sol for inj
10 x 1
-
Rx
Intramuskulær bruk, Intravenøs bruk
N02AB02
Product
Pack
Reg. Nr.
Reg. Type
Reg. Date
Reg. Valid
Revocation
Company
PETHIDIN HCL 50 MG/ML sol for inj
10 x 1
01-09-2020
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X
Romania (1)Product
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Product
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Product
Pack
SPC
PIL
Company
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X
Slovenia (11)Product
Pack
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Pres.
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Company
MIALGIN 100 MG/2 ML SOL. INJ.
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
MIALGIN 100 MG/2 ML SOL. INJ.
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
DOLANTIN inj
ampule 25x100mg/2ml
-
Rx
parenteral
N02AB02
DOLANTIN 100 MG/2 ML sol for inj
5 amp 2 ml sol
-
Rx
parenteral
N02AB02
Product
Pack
Reg. Nr.
Reg. Type
Reg. Date
Reg. Valid
Revocation
Company
DOLANTIN inj
ampule 25x100mg/2ml
-
DOLANTIN 100 MG/2 ML sol for inj
5 amp 2 ml sol
-
PETHIDINE INJECTION BP 50 MG/ML sol for inj
10 amp 2 ml sol
842-227/2017
-
17-10-2017
17-10-2018
17-04-2020
PETIDIN MACARTHYS 50 MG/ML sol for inj
10 amp 2 ml sol
842-340/2018
-
04-10-2018
04-10-2019
PETIDINIJEV KLORID MERCURY 50 MG/ML sol for inj
10 amp 2 ml sol
842-373/2018
-
25-10-2018
25-10-2019
Product
Pack
Ex-fact
Wholesale
Net retail
Gr. retail
Company
DOLANTIN inj
ampule 25x100mg/2ml
DOLANTIN 100 MG/2 ML sol for inj
5 amp 2 ml sol
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X
Sweden (1)Product
Pack
Market
Pres.
Dosage
ATC
Company
DOLANTINA 50 MG/ML sol for inj
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
VÍA INTRAVENOSA, VÍA SUBCUTÁNEA, VÍA INTRAMUSCULAR
N02AB02
HIDROCLORURO DE PETIDINA ALTAN 50 MG/ML sol for inj
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
iv/im/subcut
N02AB02
Product
Pack
Reg. Nr.
Reg. Type
Reg. Date
Reg. Valid
Revocation
Company
DOLANTINA 50 MG/ML sol for inj
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
HIDROCLORURO DE PETIDINA ALTAN 50 MG/ML sol for inj
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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13-10-2010
13-10-2010
13-10-2010
13-10-2010
13-10-2010
13-10-2010
13-10-2010
Product
Pack
SPC
PIL
Company
DOLANTINA 50 MG/ML sol for inj
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
HIDROCLORURO DE PETIDINA ALTAN 50 MG/ML sol for inj
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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X
Switzerland (6)Product
Pack
Market
Pres.
Dosage
ATC
Company
Product
Pack
Reg. Nr.
Reg. Type
Reg. Date
Reg. Valid
Revocation
Company
PETIDIN MEDA (FD PETIDIN PHARMACIA) 50 MG/ML sol for inj
Nationell decentral eller ömsesidig
06-12-1974
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X
Product
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Company
Product
Pack
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Company
PETHIDIN HCI SINTETICA 50 MG/ML SOLUZIONE INIETTABILE -
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
PETHIDIN HCL 25 MG/ML BICHSEL sol for inj
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
PETHIDIN HCL 50 MG/ML BICHSEL sol for inj
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
PETHIDIN HCL AMINO 100 MG/2 ML sol for inj
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
PETHIDIN HCL AMINO 50 MG/1 ML sol for inj
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
PETHIDIN STREULI sol for inj
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
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