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

mepivacaine

North America

Canada (6)
X
Product
Pack
Market
Pres.
Dosage
ATC
Company
Ethical
BLOCK/INFILTRATION
N01BB03
Ethical
Ethical
epid/intracaudal
N01BB03
Ethical
epid/intracaudal
N01BB03
Ethical
BLOCK/INFILTRATION
N01BB03
Ethical
subcut
N01BB03
Ethical
BLOCK/INFILTRATION
N01BB03
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United States (18)
X
Product
Pack
Market
Pres.
Dosage
ATC
Company
N
INJECTION
N01BB03
Y
Rx
INJECTION
N01BB03
Y
Rx
INJECTION
N01BB03
Y
Rx
INJECTION
N01BB03
Y
Rx
INJECTION
N01BB03
Y
Rx
INJECTION
N01BB03
N
INJECTION
N01BB03
Y
Rx
INJECTION
N01BB03
Y
Rx
INJECTION
N01BB03
Y
Rx
INJECTION
N01BB03
Y
Rx
INJECTION
N01BB03
Product
Pack
Reg. Nr.
Reg. Type
Reg. Date
Reg. Valid
Revocation
Company
84777/2
ANDA
18-04-1982
12125/3
NDA
01-01-1982
12250/5
NDA
01-01-1982
12250/1
NDA
01-01-1982
12250/2
NDA
01-01-1982
80925/1
ANDA
01-01-1982
88769/1
ANDA
20-11-1984
88770/1
ANDA
20-11-1984
83559/1
ANDA
01-01-1982
40806/1
ANDA
28-04-2008
89407/1
ANDA
01-12-1986
89410/1
ANDA
01-12-1986
88653/1
ANDA
21-08-1984
89408/1
ANDA
01-12-1986
89406/1
ANDA
01-12-1986
89409/1
ANDA
01-12-1986
88387/1
ANDA
10-10-1984
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Europe

Austria (9)
X
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Belgium (8)
X
Product
Pack
Market
Pres.
Dosage
ATC
Company
10 mL
20 mL
20 mL
-
Y
Y


epid/perineural/epilesional
N01BB03
10 mL
2 mL
20 mL
20 mL
5 mL
-
-
Y
Y
-




epid/perineural/epilesional
N01BB03
1,7 mL
Y
dental
N01BB03
20 mL
Y
epid/perineural/epilesional
N01BB03
20 mL
Y
epid/perineural/epilesional
N01BB03
1,7 mL
2,2 mL
Y
-

infiltration/perineural
N01BB03
Product
Pack
Reg. Nr.
Reg. Type
Reg. Date
Reg. Valid
Revocation
Company
10 mL
20 mL
20 mL
BE500160
BE500177
BE500177
-
-
-
10 mL
2 mL
20 mL
20 mL
5 mL
BE500204
BE500186
BE500213
BE500213
BE500195
-
-
-
-
-
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Croatia (1)
X
Product
Pack
Market
Pres.
Dosage
ATC
Company
50 uložaka 1,8 ml otopina
50 uložaka 2,2 ml otopina
T
T
Rx
Rx
-
N01BB03
Product
Pack
Reg. Nr.
Reg. Type
Reg. Date
Reg. Valid
Revocation
Company
50 uložaka 1,8 ml otopina
50 uložaka 2,2 ml otopina
HR-H-061239038-01
HR-H-061239038-02
27-08-2018
27-08-2018
01-02-2019
01-02-2019
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Czechia (1)
X
Product
Pack
Market
Pres.
Dosage
ATC
Company
30MG/ML 10X1,8ML
Y
infiltration
N01BB03
Product
Pack
Reg. Nr.
Reg. Type
Reg. Date
Reg. Valid
Revocation
Company
30MG/ML 10X1,8ML
-
Product
Pack
Ex-fact
Wholesale
Net retail
Gr. retail
Company
30MG/ML 10X1,8ML
0
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Denmark (5)
X
Product
Pack
Reg. Nr.
Reg. Type
Reg. Date
Reg. Valid
Revocation
Company
28101001756
NP
05-12-1956
28101001856
NP
05-12-1956
28101592994
MRP
15-03-1995
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Hungary (1)
X
Product
Pack
Market
Pres.
Dosage
ATC
Company
50x cartridge
N
Rx
parenteral
N01BB03
Product
Pack
Reg. Nr.
Reg. Type
Reg. Date
Reg. Valid
Revocation
Company
50x cartridge
OGYI-T-05761/01
01-01-1997
Product
Pack
Ex-fact
Wholesale
Net retail
Gr. retail
Company
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Iceland (3)
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
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Ireland (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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Lithuania (2)
X
Product
Pack
Market
Pres.
Dosage
ATC
Company
1,7 ml N50 užtaisas
Rx
oromucosal
N01BB03
1,7 ml N50 užtaisas
2,2 ml N50 užtaisas
Rx
Rx
perineural
N01BB03
Product
Pack
Reg. Nr.
Reg. Type
Reg. Date
Reg. Valid
Revocation
Company
1,7 ml N50 užtaisas
LT/1/04/3406/001
NP
10-02-2004
1,7 ml N50 užtaisas
2,2 ml N50 užtaisas
LT/1/01/2595/002
LT/1/01/2595/003
MRP
MRP
16-05-2001
16-05-2001
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Malta (1)
X
Product
Pack
Market
Pres.
Dosage
ATC
Company
Product
Pack
Reg. Nr.
Reg. Type
Reg. Date
Reg. Valid
Revocation
Company
MA035/00401
03-08-2007
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Poland (3)
X
Product
Pack
Market
Pres.
Dosage
ATC
Company
10 amp-syr 1,8 ml
50 amp-syr 1,8 ml
Rp
Rp
-
N01BB03
50 amp 1,7 ml
Rp
-
N01BB03
50 s-amp. 1,8 ml
50 wkładów 1,7 ml
50 wkładów 1,8 ml
Rp
Rp
-
N01BB03
Product
Pack
Reg. Nr.
Reg. Type
Reg. Date
Reg. Valid
Revocation
Company
10 amp-syr 1,8 ml
50 amp-syr 1,8 ml
02203
02203
NP
NP
50 amp 1,7 ml
01304
NP
50 s-amp. 1,8 ml
50 wkładów 1,7 ml
50 wkładów 1,8 ml
03031
03031
03031
NP
NP
NP
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Romania (3)
X
Product
Pack
Market
Pres.
Dosage
ATC
Company
5 blister PVC/hartie a cate 10 cartuse d
-
PR
-
N01BB03
50 cartuse din sticla incolora x 1,7 ml
-
PR
-
N01BB03
50 cartuse din sticla incolora tip I x 1
-
PR
-
N01BB03
Product
Pack
Reg. Nr.
Reg. Type
Reg. Date
Reg. Valid
Revocation
Company
5 blister PVC/hartie a cate 10 cartuse d
-
50 cartuse din sticla incolora x 1,7 ml
-
50 cartuse din sticla incolora tip I x 1
-
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Slovenia (1)
X
Product
Pack
Market
Pres.
Dosage
ATC
Company
50 vložki 1,7 ml sol
N
Rx
dental
N01BB03
Product
Pack
Reg. Nr.
Reg. Type
Reg. Date
Reg. Valid
Revocation
Company
50 vložki 1,7 ml sol
10123-490/2018-4
MRP
15-02-2019
Product
Pack
Ex-fact
Wholesale
Net retail
Gr. retail
Company
50 vložki 1,7 ml sol
21,05
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Spain (13)
X
Product
Pack
Market
Pres.
Dosage
ATC
Company
1 cartucho of 1,8 ml
50 cartuchos of 1,8 ml
-
Y
Rx
Rx
VÍA SUBCUTÁNEA, VÍA INTRAMUSCULAR
N01BB03
100 amp of 5 ml
-
Rx
VÍA PERIARTICULAR, VÍA SUBCUTÁNEA, VÍA PERINEURAL, VÍA INTRADÉRMICA, VÍA INTRAARTICULAR, VÍA EPIDURAL, VÍA INTRAMUSCULAR
N01BB03
100 amp of 5 ml
-
Rx
VÍA EPIDURAL, VÍA INTRADÉRMICA, VÍA PERINEURAL, VÍA SUBCUTÁNEA
N01BB03
100 cartuchos of 1,8 ml
50 cartuchos of 1,8 ml
Y
Y
Rx
Rx
iv
N01BB03
100 amp of 10 ml
Y
Rx
VÍA SUBCUTÁNEA, VÍA PERINEURAL, VÍA PERIARTICULAR, VÍA INTRAMUSCULAR, VÍA EPIDURAL, VÍA INTRAARTICULAR
N01BB03
100 amp of 10 ml
100 amp of 5 ml
Y
Y
Rx
Rx
epid/perineural/subcut
N01BB03
1 amp of 10 ml
100 amp of 10 ml
-
Y
Rx
Rx
VÍA PERIARTICULAR, VÍA EPIDURAL, VÍA PERINEURAL, VÍA SUBCUTÁNEA, VÍA INTRAARTICULAR, VÍA INTRAMUSCULAR, VÍA INTRADÉRMICA
N01BB03
1 amp of 10 ml
1 amp of 2 ml
100 amp of 10 ml
100 amp of 2 ml
-
-
Y
Y
Rx
Rx
Rx
Rx
VÍA INTRADÉRMICA, VÍA PERINEURAL, VÍA EPIDURAL, VÍA SUBCUTÁNEA
N01BB03
1 amp of 1,8 ml
100 amp of 1,8 ml
-
Y
Rx
Rx
infiltration/perineural
N01BB03
1 amp of 10 ml
100 amp of 10 ml
-
Y
Rx
Rx
infiltration
N01BB03
1 amp of 10 ml
1 amp of 2 ml
100 amp of 10 ml
100 amp of 2 ml
-
-
-
-
Rx
Rx
Rx
Rx
infiltration
N01BB03
100 cartuchos of 1,8 ml
100 cartuchos of 1,8 ml
Y
Y
Rx
Rx
infiltration
N01BB03
50 cartuchos of 1,7 ml
Y
Rx
infiltration/perineural
N01BB03
Product
Pack
Reg. Nr.
Reg. Type
Reg. Date
Reg. Valid
Revocation
Company
1 cartucho of 1,8 ml
50 cartuchos of 1,8 ml
60605
60605
01-03-1995
01-03-1995
100 amp of 5 ml
67288
29-11-2005
100 amp of 5 ml
67289
29-11-2005
100 cartuchos of 1,8 ml
50 cartuchos of 1,8 ml
68352
68352
16-01-2007
16-01-2007
100 amp of 10 ml
100 amp of 5 ml
62606
62606
01-07-1999
01-07-1999
1 amp of 10 ml
100 amp of 10 ml
69201
69201
06-08-2007
06-08-2007
1 amp of 10 ml
1 amp of 2 ml
100 amp of 10 ml
100 amp of 2 ml
69203
69203
69203
69203
06-08-2007
06-08-2007
06-08-2007
06-08-2007
1 amp of 1,8 ml
100 amp of 1,8 ml
65298
65298
12-03-2003
12-03-2003
1 amp of 10 ml
100 amp of 10 ml
37726
37726
01-05-1962
01-05-1962
1 amp of 10 ml
1 amp of 2 ml
100 amp of 10 ml
100 amp of 2 ml
37725
37725
37725
37725
01-05-1962
01-05-1962
01-05-1962
01-05-1962
100 cartuchos of 1,8 ml
100 cartuchos of 1,8 ml
39732
39732
01-06-1964
01-06-1964
50 cartuchos of 1,7 ml
69095
11-07-2007
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Sweden (10)
X
Product
Pack
Reg. Nr.
Reg. Type
Reg. Date
Reg. Valid
Revocation
Company
Nationell decentral eller ömsesidig
13-10-1959
Nationell decentral eller ömsesidig
13-10-1959
Nationell decentral eller ömsesidig
13-10-1959
16-06-2008
Nationell decentral eller ömsesidig
19-06-1963
Nationell decentral eller ömsesidig
08-05-1987
16-06-2008
Nationell decentral eller ömsesidig
11-12-1987
16-06-2008
Nationell decentral eller ömsesidig
11-12-1987
16-06-2008
Nationell decentral eller ömsesidig
16-06-2016
Nationell decentral eller ömsesidig
16-06-2016
Nationell decentral eller ömsesidig
19-11-1999
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Switzerland (4)
X
Product
Pack
Reg. Nr.
Reg. Type
Reg. Date
Reg. Valid
Revocation
Company
48352 3
Hauptzulassung
15-08-1988
19-12-2022
48352 4
Hauptzulassung
15-08-1988
19-12-2022
48352 2
Hauptzulassung
15-08-1988
19-12-2022
38646 2
Hauptzulassung
30-07-1975
21-03-2024
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