pethidine

North America

Canada (1)
X
Product
Pack
Market
Pres.
Dosage
ATC
Company
MEPERIDINE HYDROCHLORIDE INJECTION USP 50MG/ML sol
Narcotic (CDSA I)
iv/im/subcut
N02AB02
Product
Pack
Reg. Nr.
Reg. Type
Reg. Date
Reg. Valid
Revocation
Company
MEPERIDINE HYDROCHLORIDE INJECTION USP 50MG/ML sol
00725765
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.

United States (61)
X
Product
Pack
Market
Pres.
Dosage
ATC
Company
DEMEROL syrup
N
oral
N02AB02
DEMEROL 100MG tabs
N
oral
N02AB02
DEMEROL 100MG/ML inj
Y
Rx
INJECTION
N02AB02
DEMEROL 100MG/ML inj
N
INJECTION
N02AB02
DEMEROL 25MG/ML inj
Y
Rx
INJECTION
N02AB02
DEMEROL 25MG/ML inj
N
INJECTION
N02AB02
DEMEROL 50MG tabs
N
oral
N02AB02
DEMEROL 50MG/ML inj
Y
Rx
INJECTION
N02AB02
DEMEROL 50MG/ML inj
N
INJECTION
N02AB02
DEMEROL 75MG/ML inj
Y
Rx
INJECTION
N02AB02
DEMEROL 75MG/ML inj
N
INJECTION
N02AB02
MEPERIDINE HYDROCHLORIDE 100MG tabs
N
oral
N02AB02
MEPERIDINE HYDROCHLORIDE 100MG tabs
N
oral
N02AB02
MEPERIDINE HYDROCHLORIDE 100MG tabs
N
oral
N02AB02
MEPERIDINE HYDROCHLORIDE 100MG tabs
Y
Rx
oral
N02AB02
MEPERIDINE HYDROCHLORIDE 100MG tabs
N
oral
N02AB02
MEPERIDINE HYDROCHLORIDE 100MG tabs
N
oral
N02AB02
MEPERIDINE HYDROCHLORIDE 100MG tabs
N
N

oral
N02AB02
MEPERIDINE HYDROCHLORIDE 100MG tabs
N
oral
N02AB02
MEPERIDINE HYDROCHLORIDE 100MG tabs
N
oral
N02AB02
MEPERIDINE HYDROCHLORIDE 100MG/ML inj
N
INJECTION
N02AB02
MEPERIDINE HYDROCHLORIDE 100MG/ML inj
N
INJECTION
N02AB02
MEPERIDINE HYDROCHLORIDE 100MG/ML inj
N
N
N


INJECTION
N02AB02
MEPERIDINE HYDROCHLORIDE 100MG/ML inj
N
INJECTION
N02AB02
MEPERIDINE HYDROCHLORIDE 100MG/ML inj
N
INJECTION
N02AB02
MEPERIDINE HYDROCHLORIDE 100MG/ML inj
Y
Y
Rx
Rx
INJECTION
N02AB02
MEPERIDINE HYDROCHLORIDE 10MG/ML inj
N
INJECTION
N02AB02
MEPERIDINE HYDROCHLORIDE 150MG tabs
N
oral
N02AB02
MEPERIDINE HYDROCHLORIDE 25MG/ML inj
N
INJECTION
N02AB02
MEPERIDINE HYDROCHLORIDE 25MG/ML inj
N
INJECTION
N02AB02
MEPERIDINE HYDROCHLORIDE 25MG/ML inj
N
INJECTION
N02AB02
MEPERIDINE HYDROCHLORIDE 25MG/ML inj
Y
Y
Rx
Rx
INJECTION
N02AB02
MEPERIDINE HYDROCHLORIDE 50MG tabs
N
oral
N02AB02
MEPERIDINE HYDROCHLORIDE 50MG tabs
N
oral
N02AB02
MEPERIDINE HYDROCHLORIDE 50MG tabs
N
oral
N02AB02
MEPERIDINE HYDROCHLORIDE 50MG tabs
Y
Rx
oral
N02AB02
MEPERIDINE HYDROCHLORIDE 50MG tabs
N
oral
N02AB02
MEPERIDINE HYDROCHLORIDE 50MG tabs
N
oral
N02AB02
MEPERIDINE HYDROCHLORIDE 50MG tabs
N
N

oral
N02AB02
MEPERIDINE HYDROCHLORIDE 50MG tabs
N
oral
N02AB02
MEPERIDINE HYDROCHLORIDE 50MG tabs
N
oral
N02AB02
MEPERIDINE HYDROCHLORIDE 50MG tabs
N
oral
N02AB02
MEPERIDINE HYDROCHLORIDE 50MG/5ML syrup
Y
Rx
oral
N02AB02
MEPERIDINE HYDROCHLORIDE 50MG/ML inj
N
N

INJECTION
N02AB02
MEPERIDINE HYDROCHLORIDE 50MG/ML inj
N
INJECTION
N02AB02
MEPERIDINE HYDROCHLORIDE 50MG/ML inj
N
N
N


INJECTION
N02AB02
MEPERIDINE HYDROCHLORIDE 50MG/ML inj
N
INJECTION
N02AB02
MEPERIDINE HYDROCHLORIDE 50MG/ML inj
N
INJECTION
N02AB02
MEPERIDINE HYDROCHLORIDE 50MG/ML inj
Y
Y
Rx
Rx
INJECTION
N02AB02
MEPERIDINE HYDROCHLORIDE 75MG tabs
N
oral
N02AB02
MEPERIDINE HYDROCHLORIDE 75MG/ML inj
N
INJECTION
N02AB02
MEPERIDINE HYDROCHLORIDE 75MG/ML inj
N
INJECTION
N02AB02
MEPERIDINE HYDROCHLORIDE 75MG/ML inj
N
INJECTION
N02AB02
MEPERIDINE HYDROCHLORIDE 75MG/ML inj
N
INJECTION
N02AB02
MEPERIDINE HYDROCHLORIDE 75MG/ML inj
Y
Y
Rx
Rx
INJECTION
N02AB02
MEPERIDINE HYDROCHLORIDE PRESERVATIVE FREE 10MG/ML inj
N
INJECTION
N02AB02
MEPERIDINE HYDROCHLORIDE PRESERVATIVE FREE 10MG/ML inj
N
INJECTION
N02AB02
MEPERIDINE HYDROCHLORIDE PRESERVATIVE FREE 10MG/ML inj
N
INJECTION
N02AB02
MEPERIDINE HYDROCHLORIDE PRESERVATIVE FREE 10MG/ML inj
N
INJECTION
N02AB02
MEPERIDINE HYDROCHLORIDE PRESERVATIVE FREE 10MG/ML inj
N
INJECTION
N02AB02
MEPERIDINE HYDROCHLORIDE PRESERVATIVE FREE 10MG/ML inj
Y
Rx
INJECTION
N02AB02
Product
Pack
Reg. Nr.
Reg. Type
Reg. Date
Reg. Valid
Revocation
Company
DEMEROL syrup
5010/5
NDA
01-01-1982
DEMEROL 100MG tabs
5010/4
NDA
01-01-1982
DEMEROL 100MG/ML inj
21171/4
NDA
01-01-1982
DEMEROL 100MG/ML inj
5010/3
NDA
01-01-1982
DEMEROL 25MG/ML inj
21171/1
NDA
01-01-1982
DEMEROL 25MG/ML inj
5010/7
NDA
01-01-1982
DEMEROL 50MG tabs
5010/1
NDA
01-01-1982
DEMEROL 50MG/ML inj
21171/2
NDA
01-01-1982
DEMEROL 50MG/ML inj
5010/2
NDA
01-01-1982
DEMEROL 75MG/ML inj
21171/3
NDA
01-01-1982
DEMEROL 75MG/ML inj
5010/9
NDA
01-01-1982
MEPERIDINE HYDROCHLORIDE 100MG tabs
40893/3
ANDA
24-06-2009
MEPERIDINE HYDROCHLORIDE 100MG tabs
88640/1
ANDA
19-09-1984
MEPERIDINE HYDROCHLORIDE 100MG tabs
40318/2
ANDA
05-10-1999
MEPERIDINE HYDROCHLORIDE 100MG tabs
40331/2
ANDA
28-05-1999
MEPERIDINE HYDROCHLORIDE 100MG tabs
40110/2
ANDA
12-03-1997
MEPERIDINE HYDROCHLORIDE 100MG tabs
40352/2
ANDA
13-06-2000
MEPERIDINE HYDROCHLORIDE 100MG tabs
80448/2
40446/2
ANDA
ANDA
01-01-1982
08-08-2002
MEPERIDINE HYDROCHLORIDE 100MG tabs
40191/2
ANDA
17-12-1998
MEPERIDINE HYDROCHLORIDE 100MG tabs
40186/2
ANDA
30-06-1997
MEPERIDINE HYDROCHLORIDE 100MG/ML inj
80386/1
ANDA
01-01-1982
MEPERIDINE HYDROCHLORIDE 100MG/ML inj
88282/1
ANDA
15-06-1984
MEPERIDINE HYDROCHLORIDE 100MG/ML inj
89788/1
89787/1
89786/1
ANDA
ANDA
ANDA
31-03-1989
31-03-1989
31-03-1989
MEPERIDINE HYDROCHLORIDE 100MG/ML inj
80364/1
ANDA
01-01-1982
MEPERIDINE HYDROCHLORIDE 100MG/ML inj
73445/1
ANDA
17-03-1992
MEPERIDINE HYDROCHLORIDE 100MG/ML inj
80445/4
80455/10
ANDA
ANDA
01-01-1982
01-01-1982
MEPERIDINE HYDROCHLORIDE 10MG/ML inj
86332/1
ANDA
01-01-1982
MEPERIDINE HYDROCHLORIDE 150MG tabs
40893/4
ANDA
24-06-2009
MEPERIDINE HYDROCHLORIDE 25MG/ML inj
80388/1
ANDA
01-01-1982
MEPERIDINE HYDROCHLORIDE 25MG/ML inj
88279/1
ANDA
15-06-1984
MEPERIDINE HYDROCHLORIDE 25MG/ML inj
89781/1
ANDA
31-03-1989
MEPERIDINE HYDROCHLORIDE 25MG/ML inj
80445/1
80455/7
ANDA
ANDA
01-01-1982
01-01-1982
MEPERIDINE HYDROCHLORIDE 50MG tabs
40893/1
ANDA
24-06-2009
MEPERIDINE HYDROCHLORIDE 50MG tabs
88639/1
ANDA
02-07-1984
MEPERIDINE HYDROCHLORIDE 50MG tabs
40318/1
ANDA
05-10-1999
MEPERIDINE HYDROCHLORIDE 50MG tabs
40331/1
ANDA
28-05-1999
MEPERIDINE HYDROCHLORIDE 50MG tabs
40110/1
ANDA
12-03-1997
MEPERIDINE HYDROCHLORIDE 50MG tabs
40352/1
ANDA
13-06-2000
MEPERIDINE HYDROCHLORIDE 50MG tabs
80448/1
40446/1
ANDA
ANDA
01-01-1982
08-08-2002
MEPERIDINE HYDROCHLORIDE 50MG tabs
40191/1
ANDA
17-12-1998
MEPERIDINE HYDROCHLORIDE 50MG tabs
40186/1
ANDA
30-06-1997
MEPERIDINE HYDROCHLORIDE 50MG tabs
80454/1
ANDA
01-01-1982
MEPERIDINE HYDROCHLORIDE 50MG/5ML syrup
88744/1
ANDA
30-01-1985
MEPERIDINE HYDROCHLORIDE 50MG/ML inj
80387/1
80385/1
ANDA
ANDA
01-01-1982
01-01-1982
MEPERIDINE HYDROCHLORIDE 50MG/ML inj
88280/1
ANDA
15-06-1984
MEPERIDINE HYDROCHLORIDE 50MG/ML inj
89784/1
89783/1
89782/1
ANDA
ANDA
ANDA
31-03-1989
31-03-1989
31-03-1989
MEPERIDINE HYDROCHLORIDE 50MG/ML inj
80364/2
ANDA
01-01-1982
MEPERIDINE HYDROCHLORIDE 50MG/ML inj
73444/1
ANDA
17-03-1992
MEPERIDINE HYDROCHLORIDE 50MG/ML inj
80445/2
80455/8
ANDA
ANDA
01-01-1982
01-01-1982
MEPERIDINE HYDROCHLORIDE 75MG tabs
40893/2
ANDA
24-06-2009
MEPERIDINE HYDROCHLORIDE 75MG/ML inj
80389/1
ANDA
01-01-1982
MEPERIDINE HYDROCHLORIDE 75MG/ML inj
88281/1
ANDA
15-06-1984
MEPERIDINE HYDROCHLORIDE 75MG/ML inj
89785/1
ANDA
31-03-1989
MEPERIDINE HYDROCHLORIDE 75MG/ML inj
80364/3
ANDA
01-01-1982
MEPERIDINE HYDROCHLORIDE 75MG/ML inj
80445/3
80455/9
ANDA
ANDA
01-01-1982
01-01-1982
MEPERIDINE HYDROCHLORIDE PRESERVATIVE FREE 10MG/ML inj
40305/1
ANDA
10-03-1999
MEPERIDINE HYDROCHLORIDE PRESERVATIVE FREE 10MG/ML inj
88432/1
ANDA
16-08-1984
MEPERIDINE HYDROCHLORIDE PRESERVATIVE FREE 10MG/ML inj
81309/1
ANDA
30-08-1993
MEPERIDINE HYDROCHLORIDE PRESERVATIVE FREE 10MG/ML inj
40163/1
ANDA
12-05-1997
MEPERIDINE HYDROCHLORIDE PRESERVATIVE FREE 10MG/ML inj
73443/1
ANDA
17-03-1992
MEPERIDINE HYDROCHLORIDE PRESERVATIVE FREE 10MG/ML inj
81002/1
ANDA
30-07-1993
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Europe

Austria (1)
X
Product
Pack
Market
Pres.
Dosage
ATC
Company
ALODAN 50 MG/ML sol for inj
Rx
-
N02AB02
Product
Pack
Reg. Nr.
Reg. Type
Reg. Date
Reg. Valid
Revocation
Company
ALODAN 50 MG/ML sol for inj
7063
13-03-1953
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 (2)
X
Product
Pack
Market
Pres.
Dosage
ATC
Company
PETHISOM 100 MG/2 ML sol for inj
2 mL
2 mL
Y
N

iv/im/subcut
N02AB02
PETHISOM 50 MG/1 ML sol for inj
1 mL
1 mL
Y
-

iv/im/subcut
N02AB02
Product
Pack
Reg. Nr.
Reg. Type
Reg. Date
Reg. Valid
Revocation
Company
PETHISOM 100 MG/2 ML sol for inj
2 mL
2 mL
BE489653
BE489653
-
-
PETHISOM 50 MG/1 ML sol for inj
1 mL
1 mL
BE489644
BE489644
-
-
Product
Pack
Ex-fact
Wholesale
Net retail
Gr. retail
Company
PETHISOM 100 MG/2 ML sol for inj
2 mL
2 mL
PETHISOM 50 MG/1 ML sol for inj
1 mL
1 mL
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Bosnia and Herzegovina (0)
No result.
Croatia (0)
No result.
Czechia (1)
X
Product
Pack
Market
Pres.
Dosage
ATC
Company
DOLSIN 50MG/ML sol for inj
50MG/ML 10X1ML
50MG/ML 10X2ML
Y
Y
iv/im/subcut
N02AB02
Product
Pack
Reg. Nr.
Reg. Type
Reg. Date
Reg. Valid
Revocation
Company
DOLSIN 50MG/ML sol for inj
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
DOLSIN 50MG/ML sol for inj
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
PETIDIN DAK 100 MG supp
-
-
N02AB02
PETIDIN DAK 25 MG tabs
-
-
N02AB02
Product
Pack
Reg. Nr.
Reg. Type
Reg. Date
Reg. Valid
Revocation
Company
PETIDIN DAK 100 MG supp
28100743376
NP
01-08-1977
PETIDIN DAK 25 MG tabs
28100743476
NP
01-08-1977
Product
Pack
Ex-fact
Wholesale
Net retail
Gr. retail
Company
PETIDIN DAK 100 MG supp
PETIDIN DAK 25 MG tabs
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.

Finland (0)
No result.
Hungary (2)
X
Product
Pack
Market
Pres.
Dosage
ATC
Company
DOLARGAN sol for inj
25x2ml amp
5x2ml amp
Y
Y
Rx
Rx
parenteral
N02AB02
PETHIDINE PANPHARMA 50 MG/ML sol for inj
10x2ml amp
N
Rx
-
N02AB02
Product
Pack
Reg. Nr.
Reg. Type
Reg. Date
Reg. Valid
Revocation
Company
DOLARGAN sol for inj
25x2ml amp
5x2ml amp
OGYI-T-12707/02
OGYI-T-12707/01
01-01-1939
01-01-1939
01-02-2021
01-02-2021
PETHIDINE PANPHARMA 50 MG/ML sol for inj
10x2ml amp
OGYI-T-23784/01
25-11-2020
Product
Pack
Ex-fact
Wholesale
Net retail
Gr. retail
Company
DOLARGAN sol for inj
25x2ml amp
5x2ml amp
0
0
0
0
0
0
0
0
PETHIDINE PANPHARMA 50 MG/ML sol for inj
10x2ml amp
0
0
0
0
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.

Iceland (0)
No result.
Ireland (2)
X
Product
Pack
Market
Pres.
Dosage
ATC
Company
PETHIDINE HYDROCHLORIDE 50 MG/ML sol for inj
N
Rx
iv/im/subcut
N02AB02
PETHIDINE HYDROCHLORIDE 50MG/ML 50 MG/ML sol for inj
Y
Rx
iv/im/subcut
N02AB02
Product
Pack
Reg. Nr.
Reg. Type
Reg. Date
Reg. Valid
Revocation
Company
PETHIDINE HYDROCHLORIDE 50 MG/ML sol for inj
PA2315/207/001
17-02-2006
PETHIDINE HYDROCHLORIDE 50MG/ML 50 MG/ML sol for inj
PA0073/014/001
01-04-1978
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.

Lithuania (2)
X
Product
Pack
Market
Pres.
Dosage
ATC
Company
DOLOBLOK 50 MG/ML sol for inj
1 ml N10 amp
2 ml N10 amp
Rx
Rx
iv/im/subcut
N02AB02
DOLSIN 50 MG/ML sol for inj
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
DOLOBLOK 50 MG/ML sol for inj
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
DOLSIN 50 MG/ML sol for inj
1 ml N10 amp
2 ml N10 amp
LT/L/21/1501/001
LT/L/21/1501/002
PI
PI
29-03-2021
29-03-2021
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Malta (9)
X
Product
Pack
Market
Pres.
Dosage
ATC
Company
PETHIDINE BP 5%W/V (50MG/ML) sol for inj
Rx
-
N02AB02
PETHIDINE BP 5%W/V (100MG/2ML) sol for inj
Rx
-
N02AB02
PETHIDINE 50MG/ML sol for inj
Rx
-
N02AB02
PETHIDINE HYDROCHLORIDE 50MG tabs
Rx
-
N02AB02
PETHIDINE HYDROCHLORIDE 50MG tabs
Rx
-
N02AB02
PETHIDINE HYDROCHLORIDE 50MG/ML sol for inj
Rx
-
N02AB02
PETHIDINE HYDROCHLORIDE 50MG/ML (1ML) sol for inj
Rx
-
N02AB02
PETHIDINE HYDROCHLORIDE 50MG/ML (2ML) sol for inj
Rx
-
N02AB02
PETHIDINE HYDROCHLORIDE MOLTENI 100MG/2ML sol for inj
Rx
-
N02AB02
Product
Pack
Reg. Nr.
Reg. Type
Reg. Date
Reg. Valid
Revocation
Company
PETHIDINE BP 5%W/V (50MG/ML) sol for inj
MA050/00301
29-04-2007
PETHIDINE BP 5%W/V (100MG/2ML) sol for inj
MA050/00302
29-04-2007
PETHIDINE 50MG/ML sol for inj
PI565/43401B
13-05-2019
PETHIDINE HYDROCHLORIDE 50MG tabs
AA561/01001
13-10-2015
PETHIDINE HYDROCHLORIDE 50MG tabs
AA565/43402
18-03-2020
PETHIDINE HYDROCHLORIDE 50MG/ML sol for inj
PI565/43401A
02-04-2019
PETHIDINE HYDROCHLORIDE 50MG/ML (1ML) sol for inj
MA079/01201
16-04-2007
PETHIDINE HYDROCHLORIDE 50MG/ML (2ML) sol for inj
MA079/01202
16-04-2007
PETHIDINE HYDROCHLORIDE MOLTENI 100MG/2ML sol for inj
AA500/00501
03-01-2019
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.

Netherlands (1)
X
Product
Pack
Market
Pres.
Dosage
ATC
Company
PETHIDINE HCL TEVA 50 MG/ML sol for inj
-
Rx
parenteral
N02AB02
Product
Pack
Reg. Nr.
Reg. Type
Reg. Date
Reg. Valid
Revocation
Company
PETHIDINE HCL TEVA 50 MG/ML sol for inj
RVG 03561
-
01-12-1982
Product
Pack
SPC
PIL
Company
PETHIDINE HCL TEVA 50 MG/ML sol for inj
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.

Norway (2)
X
Product
Pack
Market
Pres.
Dosage
ATC
Company
DOLCONTRAL 100 MG Stikkpille
10
-
Rx
rectal
N02AB02
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
DOLCONTRAL 100 MG Stikkpille
10
15-07-2020
PETHIDIN HCL 50 MG/ML sol for inj
10 x 1
01-09-2020
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.

Poland (1)
X
Product
Pack
Market
Pres.
Dosage
ATC
Company
DOLCONTRAL 50 MG/ML sol for inj
10 amp 1 ml
10 amp 2 ml
-
-
Rx
Rx
-
N02AB02
Product
Pack
Reg. Nr.
Reg. Type
Reg. Date
Reg. Valid
Revocation
Company
DOLCONTRAL 50 MG/ML sol for inj
10 amp 1 ml
10 amp 2 ml
03546
03546
NP
NP
Product
Pack
SPC
PIL
Company
DOLCONTRAL 50 MG/ML sol for inj
10 amp 1 ml
10 amp 2 ml
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.

Romania (1)
X
Product
Pack
Market
Pres.
Dosage
ATC
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
-
-
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
-
-
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Slovenia (11)
X
Product
Pack
Market
Pres.
Dosage
ATC
Company
ALODAN 50 MG/ML sol for inj
5 amp 2 ml sol
N
-
N02AB02
DOLANTIN inj
ampule 25x100mg/2ml
-
Rx
parenteral
N02AB02
DOLANTIN 100 MG/2 ML sol for inj
5 amp 2 ml sol
-
Rx
parenteral
N02AB02
DOLANTIN 100 MG/2 ML sol for inj
5 ampul 2 ml sol
N
-
N02AB02
DOLANTIN 50 MG/ML sol for inj
5 amp 2 ml sol
-
-
N02AB02
DOLCONTRAL 50 MG/ML sol for inj
10 amp 2 ml sol
-
-
N02AB02
DOLSIN 50 MG/ML sol for inj
10 amp 2 ml sol
N
-
N02AB02
PETHIDINE HYDROCHLORIDE 50 MG/ML sol for inj
10 amp 2 ml
-
-
N02AB02
PETHIDINE INJECTION BP 50 MG/ML sol for inj
10 amp 2 ml sol
-
-
N02AB02
PETIDIN MACARTHYS 50 MG/ML sol for inj
10 amp 2 ml sol
-
-
N02AB02
PETIDINIJEV KLORID MERCURY 50 MG/ML sol for inj
10 amp 2 ml sol
-
-
N02AB02
Product
Pack
Reg. Nr.
Reg. Type
Reg. Date
Reg. Valid
Revocation
Company
ALODAN 50 MG/ML sol for inj
5 amp 2 ml sol
842-283/2020
-
28-08-2020
28-08-2021
DOLANTIN inj
ampule 25x100mg/2ml
-
DOLANTIN 100 MG/2 ML sol for inj
5 amp 2 ml sol
-
DOLANTIN 100 MG/2 ML sol for inj
5 ampul 2 ml sol
/
-
22-01-2016
21-01-2017
DOLANTIN 50 MG/ML sol for inj
5 amp 2 ml sol
/
-
04-01-2016
04-01-2017
DOLCONTRAL 50 MG/ML sol for inj
10 amp 2 ml sol
842-117/2019
-
11-03-2019
11-03-2020
DOLSIN 50 MG/ML sol for inj
10 amp 2 ml sol
842-374/2020
-
17-11-2020
17-11-2021
PETHIDINE HYDROCHLORIDE 50 MG/ML sol for inj
10 amp 2 ml
842-306/2016
-
16-01-2017
16-01-2018
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
ALODAN 50 MG/ML sol for inj
5 amp 2 ml sol
7,85
DOLANTIN inj
ampule 25x100mg/2ml
DOLANTIN 100 MG/2 ML sol for inj
5 amp 2 ml sol
DOLANTIN 100 MG/2 ML sol for inj
5 ampul 2 ml sol
DOLANTIN 50 MG/ML sol for inj
5 amp 2 ml sol
DOLCONTRAL 50 MG/ML sol for inj
10 amp 2 ml sol
DOLSIN 50 MG/ML sol for inj
10 amp 2 ml sol
11,14
PETHIDINE HYDROCHLORIDE 50 MG/ML sol for inj
10 amp 2 ml
PETHIDINE INJECTION BP 50 MG/ML sol for inj
10 amp 2 ml sol
PETIDIN MACARTHYS 50 MG/ML sol for inj
10 amp 2 ml sol
PETIDINIJEV KLORID MERCURY 50 MG/ML sol for inj
10 amp 2 ml sol
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Spain (2)
X
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
Y
Y
Y
Y
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
-
-
Y
Y
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
24245
24245
24245
24245
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
72848
72848
72848
72848
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
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
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Sweden (1)
X
Product
Pack
Market
Pres.
Dosage
ATC
Company
PETIDIN MEDA (FD PETIDIN PHARMACIA) 50 MG/ML sol for inj
Rx
-
N02AB02
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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Switzerland (6)
X
Product
Pack
Market
Pres.
Dosage
ATC
Company
PETHIDIN HCI SINTETICA 50 MG/ML SOLUZIONE INIETTABILE -
-
-
A
A
-
N02AB02
PETHIDIN HCL 25 MG/ML BICHSEL sol for inj
-
-
A
A
-
N02AB02
PETHIDIN HCL 50 MG/ML BICHSEL sol for inj
-
-
A
A
-
N02AB02
PETHIDIN HCL AMINO 100 MG/2 ML sol for inj
-
-
A
A
-
N02AB02
PETHIDIN HCL AMINO 50 MG/1 ML sol for inj
-
-
A
A
-
N02AB02
PETHIDIN STREULI sol for inj
-
-
-
A
A
A
-
N02AB02
Product
Pack
Reg. Nr.
Reg. Type
Reg. Date
Reg. Valid
Revocation
Company
PETHIDIN HCI SINTETICA 50 MG/ML SOLUZIONE INIETTABILE -
52109 1
52109 1
Hauptzulassung
Hauptzulassung
16-02-1994
16-02-1994
22-02-2024
22-02-2024
PETHIDIN HCL 25 MG/ML BICHSEL sol for inj
53572 1
53572 1
Hauptzulassung
Hauptzulassung
14-12-1998
14-12-1998
22-02-2024
22-02-2024
PETHIDIN HCL 50 MG/ML BICHSEL sol for inj
53572 2
53572 2
Hauptzulassung
Hauptzulassung
14-12-1998
14-12-1998
22-02-2024
22-02-2024
PETHIDIN HCL AMINO 100 MG/2 ML sol for inj
13369 1
13369 1
Hauptzulassung
Hauptzulassung
22-01-1947
22-01-1947
20-12-2022
20-12-2022
PETHIDIN HCL AMINO 50 MG/1 ML sol for inj
13369 2
13369 2
Hauptzulassung
Hauptzulassung
22-01-1947
22-01-1947
20-12-2022
20-12-2022
PETHIDIN STREULI sol for inj
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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