tetanus toxoid, combinations with diphtheria toxoid

North America

Canada (1)
X
Product
Pack
Market
Pres.
Dosage
ATC
Company
TD ADSORBED (2LF+5LF)/0.5ML susp
Schedule D
im
J07AM51
Product
Pack
Reg. Nr.
Reg. Type
Reg. Date
Reg. Valid
Revocation
Company
TD ADSORBED (2LF+5LF)/0.5ML susp
00514462
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United States (0)
No result.

Europe

Austria (3)
X
Product
Pack
Market
Pres.
Dosage
ATC
Company
DITEBOOSTER susp for inj in pref syr
Rx
-
J07AM51
DT-REDUCT „MéRIEUX“ susp for inj in pref syr
Rx
-
J07AM51
TD-PUR FüR ERWACHSENE UND HERANWACHSENDE -
Rx
-
J07AM51
Product
Pack
Reg. Nr.
Reg. Type
Reg. Date
Reg. Valid
Revocation
Company
DITEBOOSTER susp for inj in pref syr
2-00320
22-02-2007
DT-REDUCT „MéRIEUX“ susp for inj in pref syr
2-00144
27-03-1995
TD-PUR FüR ERWACHSENE UND HERANWACHSENDE -
2-00234
22-03-1999
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Belgium (1)
X
Product
Pack
Market
Pres.
Dosage
ATC
Company
TEDIVAX PRO ADULTO 0,5 ML/DOSE susp for inj
0,5 mL, 1x
0,5 mL, 1x
N
-

im/subcut
J07AM51
Product
Pack
Reg. Nr.
Reg. Type
Reg. Date
Reg. Valid
Revocation
Company
TEDIVAX PRO ADULTO 0,5 ML/DOSE susp for inj
0,5 mL, 1x
0,5 mL, 1x
BE164744
BE164744
-
-
Product
Pack
Ex-fact
Wholesale
Net retail
Gr. retail
Company
TEDIVAX PRO ADULTO 0,5 ML/DOSE susp for inj
0,5 mL, 1x
0,5 mL, 1x
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Bosnia and Herzegovina (1)
X
Product
Pack
Market
Pres.
Dosage
ATC
Company
IMOVAX DT ADULT 2 IU/0.5 ML+ 20 IU/0.5 ML susp for inj in pref syr
1 napunjena šprica (staklo) sa 0,5 ml (
Rx
-
J07AM51
Product
Pack
Reg. Nr.
Reg. Type
Reg. Date
Reg. Valid
Revocation
Company
IMOVAX DT ADULT 2 IU/0.5 ML+ 20 IU/0.5 ML susp for inj in pref syr
1 napunjena šprica (staklo) sa 0,5 ml (
BIH-H-6240672-6
-
14-09-2019
13-09-2024
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Croatia (3)
X
Product
Pack
Market
Pres.
Dosage
ATC
Company
CJEPIVO PROTIV DIFTERIJE I TETANUSA SA SMANJENIM SADRžAJEM A susp for inj
1 staklena amp 1 dozom cjepiva
10 staklenih amp 1 dozom cjepiva
50 staklenih amp 1 dozom cjepiva
T
T
T
Rx
Rx
Rx
-
J07AM51
CJEPIVO PROTIV DIFTERIJE I TETANUSA SA SMANJENIM SADRžAJEM A susp for inj
1 staklena bočica 10 dose cjepiva
50 staklenih bočica 10 dose cjepiva
T
T
Rx
Rx
-
J07AM51
DIFTAVAX, , CJEPIVO PROTIV DIFTERIJE SA SMANJENIM SADRžAJEM susp for inj in pref syr
1 pref syr 0,5 ml suspenzije pričvršćeno
Y
Rx
-
J07AM51
Product
Pack
Reg. Nr.
Reg. Type
Reg. Date
Reg. Valid
Revocation
Company
CJEPIVO PROTIV DIFTERIJE I TETANUSA SA SMANJENIM SADRžAJEM A susp for inj
1 staklena amp 1 dozom cjepiva
10 staklenih amp 1 dozom cjepiva
50 staklenih amp 1 dozom cjepiva
26-04-2013
26-04-2013
26-04-2013
26-04-2018
26-04-2018
26-04-2018
CJEPIVO PROTIV DIFTERIJE I TETANUSA SA SMANJENIM SADRžAJEM A susp for inj
1 staklena bočica 10 dose cjepiva
50 staklenih bočica 10 dose cjepiva
26-04-2013
26-04-2013
26-04-2018
26-04-2018
DIFTAVAX, , CJEPIVO PROTIV DIFTERIJE SA SMANJENIM SADRžAJEM susp for inj in pref syr
1 pref syr 0,5 ml suspenzije pričvršćeno
HR-H-126128199-01
19-07-2019
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Czechia (0)
No result.
Denmark (2)
X
Product
Pack
Market
Pres.
Dosage
ATC
Company
DITEBOOSTER susp for inj in pref syr
-
-
J07AM51
DITEBOOSTER susp for inj
-
-
J07AM51
Product
Pack
Reg. Nr.
Reg. Type
Reg. Date
Reg. Valid
Revocation
Company
DITEBOOSTER susp for inj in pref syr
28103648004
MRP
21-10-2005
DITEBOOSTER susp for inj
28101482791
MRP
09-09-1993
Product
Pack
Ex-fact
Wholesale
Net retail
Gr. retail
Company
DITEBOOSTER susp for inj in pref syr
DITEBOOSTER susp 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.

Finland (1)
X
Product
Pack
Market
Pres.
Dosage
ATC
Company
DITEBOOSTER susp for inj in pref syr
0.5 ml in pre-filled syringe
10 x 0.5 ml in pre-filled syringe
20 x 0.5 ml in pre-filled syringe
5 x 0.5 ml in pre-filled syringe
N
N
N
Y
Rx
Rx
Rx
Rx
-
J07AM51
Product
Pack
Reg. Nr.
Reg. Type
Reg. Date
Reg. Valid
Revocation
Company
DITEBOOSTER susp for inj in pref syr
0.5 ml in pre-filled syringe
10 x 0.5 ml in pre-filled syringe
20 x 0.5 ml in pre-filled syringe
5 x 0.5 ml in pre-filled syringe
22158
22158
22158
22158
-
-
-
-
24-11-2006
24-11-2006
24-11-2006
24-11-2006
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Hungary (0)
No result.
Iceland (1)
X
Product
Pack
Market
Pres.
Dosage
ATC
Company
DIFTAVAX susp for inj
N
Rx
-
J07AM51
Product
Pack
Reg. Nr.
Reg. Type
Reg. Date
Reg. Valid
Revocation
Company
DIFTAVAX susp for inj
12-04-1999
Product
Pack
Ex-fact
Wholesale
Net retail
Gr. retail
Company
DIFTAVAX susp 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.

Ireland (1)
X
Product
Pack
Market
Pres.
Dosage
ATC
Company
DITEBOOSTER, IN SINGLE-DOSE VIALS OR PRE-FILLED SINGLE-DOSE susp for inj in pref syr
Y
Rx
im
J07AM51
Product
Pack
Reg. Nr.
Reg. Type
Reg. Date
Reg. Valid
Revocation
Company
DITEBOOSTER, IN SINGLE-DOSE VIALS OR PRE-FILLED SINGLE-DOSE susp for inj in pref syr
PA2160/001/001
02-02-2007
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
IMOVAX DT ADULT >=2 TV/>=20 TV/DOZėJE susp for inj
N10 (5 ml - 10 dozių x 0,5 ml) bottle
Rx
im/subcut
J07AM51
IMOVAX DT ADULT >=2 TV/>=20 TV/DOZėJE susp for inj in pref syr
0,5 ml N1 pre-filled syringe
Rx
im/subcut
J07AM51
Product
Pack
Reg. Nr.
Reg. Type
Reg. Date
Reg. Valid
Revocation
Company
IMOVAX DT ADULT >=2 TV/>=20 TV/DOZėJE susp for inj
N10 (5 ml - 10 dozių x 0,5 ml) bottle
LT/1/95/2444/001
NP
15-02-1995
IMOVAX DT ADULT >=2 TV/>=20 TV/DOZėJE susp for inj in pref syr
0,5 ml N1 pre-filled syringe
LT/1/95/2444/002
NP
15-02-1995
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Malta (2)
X
Product
Pack
Market
Pres.
Dosage
ATC
Company
CLODIVAC . DIPHTHERIA AND TETANUS ADSORBED, WITH REDUCED ANT susp for inj
Rx
-
J07AM51
IMOVAX D.T. ADULT, IN PREFILLED SYRINGE. ADSORBED DIPHTHERI susp for inj
Rx
-
J07AM51
Product
Pack
Reg. Nr.
Reg. Type
Reg. Date
Reg. Valid
Revocation
Company
CLODIVAC . DIPHTHERIA AND TETANUS ADSORBED, WITH REDUCED ANT susp for inj
AA304/00101
06-09-2012
IMOVAX D.T. ADULT, IN PREFILLED SYRINGE. ADSORBED DIPHTHERI susp for inj
MA573/01001
13-02-2007
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Netherlands (0)
No result.
Norway (1)
X
Product
Pack
Market
Pres.
Dosage
ATC
Company
DITEBOOSTER > 2 IE/DOSE/> 20 IE/DOSE susp for inj in pref syr
5 x 0.5
-
Rx
im/subcut
J07AM51
Product
Pack
Reg. Nr.
Reg. Type
Reg. Date
Reg. Valid
Revocation
Company
DITEBOOSTER > 2 IE/DOSE/> 20 IE/DOSE susp for inj in pref syr
5 x 0.5
12-05-2010
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Poland (3)
X
Product
Pack
Market
Pres.
Dosage
ATC
Company
CLODIVAC NIE MNIEJ NIż 40 IU TOKSOIDU TężCOWEGO I NIE MNIEJ susp for inj
1 amp 0,5 ml
15 amp 0,5 ml
-
-
Rx
Rx
-
J07AM51
DT-SZCZEPIONKA BłONICZO-TężCOWA ADSORBOWANA NIE MNIEJ NIż 30 susp for inj
5 amp 0,5 ml
-
Rx
-
J07AM51
TD-PUR NIE MNIEJ NIż 20 IU TOKSOIDU TężCOWEGO I NIE MNIEJ NI susp for inj
1 amp-syr 0,5 ml
10 amp-syr 0,5 ml
-
-
Rx
Rx
-
J07AM51
Product
Pack
Reg. Nr.
Reg. Type
Reg. Date
Reg. Valid
Revocation
Company
CLODIVAC NIE MNIEJ NIż 40 IU TOKSOIDU TężCOWEGO I NIE MNIEJ susp for inj
1 amp 0,5 ml
15 amp 0,5 ml
00038
00038
NP
NP
DT-SZCZEPIONKA BłONICZO-TężCOWA ADSORBOWANA NIE MNIEJ NIż 30 susp for inj
5 amp 0,5 ml
04826
NP
TD-PUR NIE MNIEJ NIż 20 IU TOKSOIDU TężCOWEGO I NIE MNIEJ NI susp for inj
1 amp-syr 0,5 ml
10 amp-syr 0,5 ml
08484
08484
NP
NP
26-04-2018
26-04-2018
Product
Pack
SPC
PIL
Company
CLODIVAC NIE MNIEJ NIż 40 IU TOKSOIDU TężCOWEGO I NIE MNIEJ susp for inj
1 amp 0,5 ml
15 amp 0,5 ml
DT-SZCZEPIONKA BłONICZO-TężCOWA ADSORBOWANA NIE MNIEJ NIż 30 susp for inj
5 amp 0,5 ml
TD-PUR NIE MNIEJ NIż 20 IU TOKSOIDU TężCOWEGO I NIE MNIEJ NI susp for inj
1 amp-syr 0,5 ml
10 amp-syr 0,5 ml
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Romania (0)
No result.
Slovenia (5)
X
Product
Pack
Market
Pres.
Dosage
ATC
Company
CEPIVO PROTI DAVICI IN TETANUSU inj (intramuscular)
1 ampula 0,5 ml
1 steklenička 10 ml
1 steklenička 5 ml
-
-
-
Rx
Rx
Rx
parenteral
J07AM51
CLODIVAC 40 IU TETANUSNEGA TOKSOIDA IN 5 IU DAVIčNEGA TOKSOI susp for inj
15 amp 0,5 ml susp za injiciranje
-
-
J07AM51
IMOVAX DT ADULT susp for inj
10 napolnjenimi injekcijskimi brizgami 0
-
-
J07AM51
TD CEPIVO - ADSORBIRANO CEPIVO PROTI TETANUSU IN DAVICI ZA O susp for inj
v naprej napolnjena brizga 0,5 ml
-
Rx
parenteral
J07AM51
TD-PUR susp for inj
1 napolnjeno injekcijsko brizgo 0,5 ml s
10 napolnjenimi injekcijskimi brizgami 0
-
N
Rx
Rx
im
J07AM51
Product
Pack
Reg. Nr.
Reg. Type
Reg. Date
Reg. Valid
Revocation
Company
CEPIVO PROTI DAVICI IN TETANUSU inj (intramuscular)
1 ampula 0,5 ml
1 steklenička 10 ml
1 steklenička 5 ml
-
-
-
CLODIVAC 40 IU TETANUSNEGA TOKSOIDA IN 5 IU DAVIčNEGA TOKSOI susp for inj
15 amp 0,5 ml susp za injiciranje
/
-
03-08-2017
03-08-2018
IMOVAX DT ADULT susp for inj
10 napolnjenimi injekcijskimi brizgami 0
842-163/2020
-
07-12-2020
07-12-2021
TD CEPIVO - ADSORBIRANO CEPIVO PROTI TETANUSU IN DAVICI ZA O susp for inj
v naprej napolnjena brizga 0,5 ml
-
TD-PUR susp for inj
1 napolnjeno injekcijsko brizgo 0,5 ml s
10 napolnjenimi injekcijskimi brizgami 0
10024-119/2015-3
10024-119/2015-3
NP
NP
29-02-2016
29-02-2016
Product
Pack
Ex-fact
Wholesale
Net retail
Gr. retail
Company
CEPIVO PROTI DAVICI IN TETANUSU inj (intramuscular)
1 ampula 0,5 ml
1 steklenička 10 ml
1 steklenička 5 ml
CLODIVAC 40 IU TETANUSNEGA TOKSOIDA IN 5 IU DAVIčNEGA TOKSOI susp for inj
15 amp 0,5 ml susp za injiciranje
IMOVAX DT ADULT susp for inj
10 napolnjenimi injekcijskimi brizgami 0
TD CEPIVO - ADSORBIRANO CEPIVO PROTI TETANUSU IN DAVICI ZA O susp for inj
v naprej napolnjena brizga 0,5 ml
TD-PUR susp for inj
1 napolnjeno injekcijsko brizgo 0,5 ml s
10 napolnjenimi injekcijskimi brizgami 0
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Spain (4)
X
Product
Pack
Market
Pres.
Dosage
ATC
Company
ANATOXAL TEDI sol for inj in pref syr
1 syringe pre-filled of 0,5 ml
-
Rx
im
J07AM51
DIFTAVAX susp for inj in pref syr
1 syringe pre-filled of 0,5 ml
Y
Rx
im
J07AM51
DITANRIX ADULTO susp for inj
1 syringe pre-filled of 0,5 ml
-
Rx
im
J07AM51
DITEBOOSTER EN JERINGA MONODOSIS PRECARGADA susp for inj in pref syr
1 syringe pre-filled of 0,5 ml
5 syringes pre-filleds of 0,5 ml
5 syringes pre-filleds of 0,5 ml
-
Y
-
Rx
Rx
Rx
im
J07AM51
Product
Pack
Reg. Nr.
Reg. Type
Reg. Date
Reg. Valid
Revocation
Company
ANATOXAL TEDI sol for inj in pref syr
1 syringe pre-filled of 0,5 ml
69769
23-04-2008
DIFTAVAX susp for inj in pref syr
1 syringe pre-filled of 0,5 ml
61025
01-05-1996
DITANRIX ADULTO susp for inj
1 syringe pre-filled of 0,5 ml
60548
01-06-1995
DITEBOOSTER EN JERINGA MONODOSIS PRECARGADA susp for inj in pref syr
1 syringe pre-filled of 0,5 ml
5 syringes pre-filleds of 0,5 ml
5 syringes pre-filleds of 0,5 ml
68579
68579
68579
06-03-2007
06-03-2007
06-03-2007
Product
Pack
SPC
PIL
Company
ANATOXAL TEDI sol for inj in pref syr
1 syringe pre-filled of 0,5 ml
DIFTAVAX susp for inj in pref syr
1 syringe pre-filled of 0,5 ml
DITANRIX ADULTO susp for inj
1 syringe pre-filled of 0,5 ml
DITEBOOSTER EN JERINGA MONODOSIS PRECARGADA susp for inj in pref syr
1 syringe pre-filled of 0,5 ml
5 syringes pre-filleds of 0,5 ml
5 syringes pre-filleds of 0,5 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.

Sweden (3)
X
Product
Pack
Market
Pres.
Dosage
ATC
Company
DITEBOOSTER susp for inj
Rx
-
J07AM51
DITEBOOSTER susp for inj in pref syr
Rx
-
J07AM51
VACCIN MOT DIFTERI OCH TETANUS susp for inj
Rx
-
J07AM51
Product
Pack
Reg. Nr.
Reg. Type
Reg. Date
Reg. Valid
Revocation
Company
DITEBOOSTER susp for inj
Nationell decentral eller ömsesidig
09-02-2001
31-05-2011
DITEBOOSTER susp for inj in pref syr
Nationell decentral eller ömsesidig
20-10-2006
VACCIN MOT DIFTERI OCH TETANUS susp for inj
Nationell decentral eller ömsesidig
16-11-1979
31-01-2006
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Switzerland (1)
X
Product
Pack
Market
Pres.
Dosage
ATC
Company
DIPHTHERIE- UND TETANUS-ADSORBATIMPFSTOFF FüR KINDER susp for inj
-
B
-
J07AM51
Product
Pack
Reg. Nr.
Reg. Type
Reg. Date
Reg. Valid
Revocation
Company
DIPHTHERIE- UND TETANUS-ADSORBATIMPFSTOFF FüR KINDER susp for inj
711 1
Hauptzulassung
19-05-2006
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