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

lidocaine, combinations

North America

Canada (18)
X
Product
Pack
Market
Pres.
Dosage
ATC
Company
Ethical
urethral
N01BB52
Ethical
BLOCK/INFILTRATION, EPIDURAL
N01BB52
Ethical
BLOCK/INFILTRATION
N01BB52
Ethical
BLOCK/INFILTRATION
N01BB52
Rx
topical
N01BB52
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United States (43)
X
Product
Pack
Market
Pres.
Dosage
ATC
Company
N
iontophoresis
N01BB52
Product
Pack
Reg. Nr.
Reg. Type
Reg. Date
Reg. Valid
Revocation
Company
20530/1
NDA
21-12-1995
89650/1
89645/1
88571/1
ANDA
ANDA
ANDA
21-06-1988
21-06-1988
13-09-1985
78772/1
89646/1
ANDA
ANDA
12-05-2008
21-06-1988
85463/1
80377/3
ANDA
ANDA
01-01-1982
01-01-1982
84729/1
ANDA
17-08-1983
84728/1
ANDA
17-08-1983
84048/1
ANDA
01-01-1982
84048/2
ANDA
01-01-1982
21381/2
21381/1
NDA
NDA
01-01-1982
01-01-1982
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Europe

Austria (10)
X
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Belgium (10)
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.

Croatia (1)
X
Product
Pack
Market
Pres.
Dosage
ATC
Company
Product
Pack
Reg. Nr.
Reg. Type
Reg. Date
Reg. Valid
Revocation
Company
100 amp 2 ml otopina
HR-H-882488094-01
17-12-2019
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Czechia (1)
X
Product
Pack
Market
Pres.
Dosage
ATC
Company
GEL 10X11ML
GEL 10X6ML
N
N
-
N01BB52
Product
Pack
Reg. Nr.
Reg. Type
Reg. Date
Reg. Valid
Revocation
Company
GEL 10X11ML
GEL 10X6ML
01/ 889/92-C
01/ 889/92-C
NP
NP
Product
Pack
Ex-fact
Wholesale
Net retail
Gr. retail
Company
GEL 10X11ML
GEL 10X6ML
0
0
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Denmark (11)
X
Product
Pack
Reg. Nr.
Reg. Type
Reg. Date
Reg. Valid
Revocation
Company
28104887111
DCP
25-06-2012
28104155907
MRP
25-03-2008
28104894511
NP
30-07-2013
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Hungary (2)
X
Product
Pack
Market
Pres.
Dosage
ATC
Company
100x2ml amp
10x10ml amp
Y
Y
Rx
Rx
parenteral
N01BB52
10x sachet
1x sachet
25x sachet
2x sachet
50x sachet
5x sachet
N
N
N
N
N
N
Rx
Rx
Rx
Rx
Rx
Rx
transdermal
N01BB52
Product
Pack
Reg. Nr.
Reg. Type
Reg. Date
Reg. Valid
Revocation
Company
100x2ml amp
10x10ml amp
OGYI-T-03050/02
OGYI-T-03050/03
01-01-1957
01-01-1957
10x sachet
1x sachet
25x sachet
2x sachet
50x sachet
5x sachet
OGYI-T-20742/04
OGYI-T-20742/01
OGYI-T-20742/05
OGYI-T-20742/02
OGYI-T-20742/06
OGYI-T-20742/03
06-02-2009
06-02-2009
06-02-2009
06-02-2009
06-02-2009
06-02-2009
Product
Pack
Ex-fact
Wholesale
Net retail
Gr. retail
Company
100x2ml amp
10x10ml amp
0
0
0
0
0
0
0
0
10x sachet
1x sachet
25x sachet
2x sachet
50x sachet
5x sachet
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 (2)
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 (9)
X
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Lithuania (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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Malta (10)
X
Product
Pack
Reg. Nr.
Reg. Type
Reg. Date
Reg. Valid
Revocation
Company
MA137/00101
28-03-2006
MA125/00101
17-04-2006
MA035/00101
30-06-2005
MA137/00301
28-03-2006
MA035/00302
01-02-2006
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Poland (17)
X
Product
Pack
Market
Pres.
Dosage
ATC
Company
1 tube 30 g
1 tube 5 g
5 tub 5 g
Rp
Rp
Rp
-
N01BB52
1 tube 5 g
5 tub 5 g
5 tub 5 g
Rp
Rp
Rp
-
N01BB52
1 tube 30 g
1 tube 5 g + 2 opatrunki okluzyjne
5 tub 5 g + 12 opatrunków okluzyjnych
Rp
Rp
Rp
-
N01BB52
1 tube 30 g
1 tube 30 g + szpatułka
1 tube 5 g + 2 opatrunki okluzyjne
5 tub 5 g + 12 opatrunków okluzyjnych
Rp
Rp
Rp
Rp
-
N01BB52
1 tube 30 g
1 tube 5 g
5 tub 5 g
Rp
Rp
Rp
-
N01BB52
1 tube 30 g
1 tube 5 g + 3 opatrunki okluzyjne
5 tub 5 g + 12 opatrunków okluzyjnych
Rp
Rp
Rp
-
N01BB52
1 tube 30 g + szpatułka
1 tube 5 g + 2 opatrunki okluzyjne
5 tub 5 g + 12 opatrunków okluzyjnych
Rp
Rp
Rp
-
N01BB52
1 tube 5 g + 2 opatrunki okluzyjne
1 tube 5 g + 3 opatrunki okluzyjne
5 tub 5 g
5 tub 5 g + 10 opatrunków okluzyjnych
Rp
Rp
Rp
Rp
-
N01BB52
2 sachet
20 sachet
OTC
Rp
-
N01BB52
1 tube 15 g
1 tube 30 g
Rp
Rp
-
N01BB52
1 plaster
2 plastry
25 plastrów
5 plastrów
Rp
Rp
Rp
Rp
-
N01BB52
50 karpul po 1,8 ml
50 s-amp. 1,8 ml
Rp
-
N01BB52
Product
Pack
Reg. Nr.
Reg. Type
Reg. Date
Reg. Valid
Revocation
Company
1 tube 30 g
1 tube 5 g
5 tub 5 g
17998
17998
17998
DCP
DCP
DCP
1 tube 5 g
5 tub 5 g
5 tub 5 g
182/11
182/11
182/11
PI
PI
PI
01-06-2021
01-06-2021
01-06-2021
1 tube 30 g
1 tube 5 g + 2 opatrunki okluzyjne
5 tub 5 g + 12 opatrunków okluzyjnych
602/12
709/15
709/15
PI
PI
PI
22-10-2017
21-10-2020
21-10-2020
1 tube 30 g
1 tube 30 g + szpatułka
1 tube 5 g + 2 opatrunki okluzyjne
5 tub 5 g + 12 opatrunków okluzyjnych
32/10
776/15
776/15
776/15
PI
PI
PI
PI
28-11-2019
19-11-2020
19-11-2020
19-11-2020
1 tube 30 g
1 tube 5 g
5 tub 5 g
62/14
5/14
5/14
PI
PI
PI
13-02-2019
13-01-2024
13-01-2024
1 tube 30 g
1 tube 5 g + 3 opatrunki okluzyjne
5 tub 5 g + 12 opatrunków okluzyjnych
03733
03733
03733
MRP
MRP
MRP
1 tube 30 g + szpatułka
1 tube 5 g + 2 opatrunki okluzyjne
5 tub 5 g + 12 opatrunków okluzyjnych
354/18
354/18
354/18
PI
PI
PI
13-12-2023
13-12-2023
13-12-2023
1 tube 5 g + 2 opatrunki okluzyjne
1 tube 5 g + 3 opatrunki okluzyjne
5 tub 5 g
5 tub 5 g + 10 opatrunków okluzyjnych
553/12
553/12
553/12
553/12
PI
PI
PI
PI
08-10-2022
08-10-2022
08-10-2022
08-10-2022
2 sachet
20 sachet
08104
08104
NP
NP
1 tube 15 g
1 tube 30 g
20451
20451
DCP
DCP
1 plaster
2 plastry
25 plastrów
5 plastrów
14748
14748
14748
14748
MRP
MRP
MRP
MRP
10 s-amp. 1,8 ml
50 wkładów 1,8 ml
02205
02205
NP
NP
50 karpul po 1,8 ml
50 s-amp. 1,8 ml
03032
03032
NP
NP
13-06-2017
13-06-2017
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Romania (1)
X
Product
Pack
Market
Pres.
Dosage
ATC
Company
1 blister x 25 seringi din PP single dos
1 blister x 5 seringi din PP single dose
-
-
PRF
PRF
-
N01BB52
Product
Pack
Reg. Nr.
Reg. Type
Reg. Date
Reg. Valid
Revocation
Company
1 blister x 25 seringi din PP single dos
1 blister x 5 seringi din PP single dose
-
-
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Slovenia (6)
X
Product
Pack
Market
Pres.
Dosage
ATC
Company
25 tubami 12,5 g gela (5 x 5 tub applica
5 tubami 12,5 g gela (5 x 1 tuba applica
-
-
Rx
Rx
urethral
N01BB52
100 ampul 1,8 ml sol
-
Rx
parenteral
N01BB52
steklenico odmerno črpalko pršilno šobo
N
Rx
oral
N01BB52
Product
Pack
Reg. Nr.
Reg. Type
Reg. Date
Reg. Valid
Revocation
Company
25 tubami 12,5 g gela (5 x 5 tub applica
5 tubami 12,5 g gela (5 x 1 tuba applica
-
-
5 vial 50 ml sol
842-300/2019
-
05-08-2019
05-08-2020
5 vial 50 ml sol
842-314/2019
-
08-08-2019
08-08-2020
5 vial 50 ml sol
842-299/2018
-
17-08-2018
17-08-2019
100 ampul 1,8 ml sol
-
steklenico odmerno črpalko pršilno šobo
103-26/2015-2
NP
11-08-2015
Product
Pack
Ex-fact
Wholesale
Net retail
Gr. retail
Company
25 tubami 12,5 g gela (5 x 5 tub applica
5 tubami 12,5 g gela (5 x 1 tuba applica
100 ampul 1,8 ml sol
steklenico odmerno črpalko pršilno šobo
20,67
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Spain (8)
X
Product
Pack
Market
Pres.
Dosage
ATC
Company
100 cartuchos of 1,8 ml
50 cartuchos of 1,8 ml
Y
Y
Rx
Rx
infiltration
N01BB52
1 amp of 1,8 ml
100 amp of 1,8 ml
-
Y
Rx
Rx
INFILTRACIÓN, VÍA PERINEURAL
N01BB52
50 cartuchos of 1,8 ml
Y
Rx
subcut
N01BB52
50 cartuchos of 1,8 ml
Y
Rx
subcut
N01BB52
1 tube of 15 g
1 tube of 30 g
Y
Y
Rx
Rx
cut
N01BB52
100 cartuchos of 1,8 ml (émbolo con cavi
100 cartuchos of 1,8 ml (émbolo plano)
Y
Y
Rx
Rx
im
N01BB52
50 cartuchos of 1,8 ml
Y
Rx
dental
N01BB52
Product
Pack
Reg. Nr.
Reg. Type
Reg. Date
Reg. Valid
Revocation
Company
100 cartuchos of 1,8 ml
50 cartuchos of 1,8 ml
66542
66542
25-01-2005
25-01-2005
1 amp of 1,8 ml
100 amp of 1,8 ml
65159
65159
15-01-2003
15-01-2003
50 cartuchos of 1,8 ml
44099
01-03-1967
50 cartuchos of 1,8 ml
44097
01-03-1967
1 tube of 15 g
1 tube of 30 g
76730
76730
06-11-2012
06-11-2012
100 cartuchos of 1,8 ml (émbolo con cavi
100 cartuchos of 1,8 ml (émbolo plano)
40858
40858
01-05-1965
01-05-1965
50 cartuchos of 1,8 ml
51081
01-03-1973
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Sweden (5)
X
Product
Pack
Reg. Nr.
Reg. Type
Reg. Date
Reg. Valid
Revocation
Company
Nationell decentral eller ömsesidig
26-01-2007
Nationell decentral eller ömsesidig
25-10-1968
30-04-2005
Nationell decentral eller ömsesidig
25-10-1968
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Switzerland (9)
X
Product
Pack
Reg. Nr.
Reg. Type
Reg. Date
Reg. Valid
Revocation
Company
42669 1
Hauptzulassung
05-02-1981
30016 2
30016 2
Hauptzulassung
Hauptzulassung
03-02-1964
03-02-1964
28-03-2024
28-03-2024
30016 3
30016 3
Hauptzulassung
Hauptzulassung
03-02-1964
03-02-1964
28-03-2024
28-03-2024
62526 1
Exportzulassung
18-11-2013
17-11-2023
20272 2
Hauptzulassung
23-08-1954
27-02-2023
20272 6
Hauptzulassung
23-08-1954
27-02-2023
20272 3
Hauptzulassung
23-08-1954
27-02-2023
20272 7
Hauptzulassung
23-08-1954
27-02-2023
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