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

doxycycline

North America

Canada (11)
X
Product
Pack
Market
Pres.
Dosage
ATC
Company
Rx
subgingival
A01AB22
Rx
oral
J01AA02
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United States (187)
X
Product
Pack
Market
Pres.
Dosage
ATC
Company
Y
Rx
periodontal
A01AB22
Y
oral
J01AA02
Y
oral
J01AA02
Y
oral
J01AA02
Y
Rx
INJECTION
J01AA02
Y
Rx
INJECTION
J01AA02
Y
Rx
INJECTION
J01AA02
Y
Rx
oral
J01AA02
N
oral
J01AA02
N
oral
J01AA02
N
oral
J01AA02
N
oral
J01AA02
N
N

INJECTION
J01AA02
Y
oral
J01AA02
Product
Pack
Reg. Nr.
Reg. Type
Reg. Date
Reg. Valid
Revocation
Company
208253/1
NDA
26-04-2016
205931/2
NDA
25-07-2014
205931/1
NDA
25-07-2014
50751/1
NDA
03-09-1998
50582/1
NDA
22-07-1985
50795/2
NDA
06-05-2005
50795/3
NDA
20-06-2008
50795/5
NDA
11-04-2013
50795/6
NDA
19-12-2014
50582/2
NDA
13-08-2001
50795/1
NDA
06-05-2005
50795/4
NDA
11-04-2013
50795/7
NDA
20-05-2016
62497/2
ANDA
15-06-1984
62581/1
ANDA
15-03-1985
62497/1
ANDA
23-08-1984
209165/2
ANDA
28-07-2017
204234/3
ANDA
05-03-2014
209396/3
ANDA
29-09-2017
65055/2
ANDA
01-12-2000
65032/2
ANDA
30-06-2000
65053/2
ANDA
22-11-2000
65041/2
ANDA
28-04-2000
205115/3
ANDA
18-02-2016
91605/3
ANDA
20-12-2011
65285/2
ANDA
08-12-2005
65377/3
ANDA
07-11-2006
65070/2
ANDA
15-12-2000
65353/3
ANDA
27-11-2006
65471/3
65356/3
ANDA
ANDA
17-04-2009
31-05-2006
209582/3
ANDA
28-09-2017
91406/1
ANDA
21-08-2012
62450/1
62569/1
ANDA
ANDA
27-10-1983
09-03-1988
207757/1
ANDA
28-09-2017
200065/1
ANDA
17-02-2011
202778/1
ANDA
08-06-2012
65055/3
ANDA
15-07-2005
91605/4
ANDA
20-12-2011
65285/4
ANDA
30-07-2008
65427/1
ANDA
07-06-2007
65070/4
ANDA
14-07-2005
209582/4
ANDA
28-09-2017
62569/2
62450/2
ANDA
ANDA
09-03-1988
27-10-1983
207757/2
ANDA
28-09-2017
204234/1
ANDA
05-03-2014
209396/1
ANDA
29-09-2017
65055/1
ANDA
01-12-2000
65032/1
ANDA
30-06-2000
65053/1
ANDA
22-11-2000
65041/1
ANDA
28-04-2000
205115/1
ANDA
18-02-2016
91605/1
ANDA
20-12-2011
65285/1
ANDA
08-12-2005
65377/1
ANDA
07-11-2006
65070/1
ANDA
15-12-2000
65353/1
ANDA
27-11-2006
65471/1
65356/1
ANDA
ANDA
17-04-2009
31-05-2006
209582/1
ANDA
28-09-2017
209165/1
ANDA
28-07-2017
204234/2
ANDA
05-03-2014
209396/2
ANDA
29-09-2017
65055/4
ANDA
18-04-2005
65053/3
ANDA
10-09-2003
205115/2
ANDA
18-02-2016
91605/2
ANDA
20-12-2011
65285/3
ANDA
30-07-2008
65377/2
ANDA
07-11-2006
65070/3
ANDA
30-12-2002
65353/2
ANDA
27-11-2006
65471/2
65356/2
ANDA
ANDA
17-04-2009
31-05-2006
209582/2
ANDA
28-09-2017
62142/2
61717/2
ANDA
ANDA
01-01-1982
01-01-1982
62434/1
ANDA
19-10-1984
61717/1
62142/1
ANDA
ANDA
01-01-1982
01-01-1982
207774/1
ANDA
31-05-2018
208818/1
ANDA
27-09-2017
50641/1
NDA
29-12-1989
50641/2
NDA
10-02-1992
50641/3
NDA
18-10-2006
50805/1
NDA
26-05-2006
50744/1
NDA
30-09-1998
50783/1
NDA
02-02-2001
50533/1
NDA
01-01-1982
50007/1
NDA
01-01-1982
50442/1
50442/2
NDA
NDA
01-01-1982
01-01-1982
50007/2
NDA
01-01-1982
50480/1
NDA
01-01-1982
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Europe

Austria (16)
X
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Belgium (10)
X
Product
Pack
Market
Pres.
Dosage
ATC
Company
260 mg
260 mg
N
-

periodontal
A01AB22
10x
20x
Y
-

oral
J01AA02
10x
20x
Y
-

oral
J01AA02
10x
Y
oral
J01AA02
10x
Y
oral
J01AA02
60 mL
N
oral
J01AA02
14x
28x
56x
-
-
Y


oral
J01AA02
Product
Pack
Reg. Nr.
Reg. Type
Reg. Date
Reg. Valid
Revocation
Company
260 mg
260 mg
BE442285
BE442285
-
-
10x
20x
BE178035
BE178035
-
-
10x
20x
BE178026
BE178026
-
-
14x
28x
56x
BE391133
BE391133
BE391133
-
-
-
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Croatia (2)
X
Product
Pack
Market
Pres.
Dosage
ATC
Company
25 caps u bočici
6 caps u bočici
T
T
Rx
Rx
-
J01AA02
5 caps in blister
Y
Rx
-
J01AA02
Product
Pack
Reg. Nr.
Reg. Type
Reg. Date
Reg. Valid
Revocation
Company
25 caps u bočici
6 caps u bočici
HR-H-507803517-02
HR-H-507803517-01
05-01-2018
05-01-2018
5 caps in blister
HR-H-515496274-01
16-03-2015
07-05-2019
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Czechia (4)
X
Product
Pack
Market
Pres.
Dosage
ATC
Company
100MG 10
Y
oral
J01AA02
200MG 10
200MG 20
Y
N
oral
J01AA02
100MG 10
100MG 20
Y
Y
oral
J01AA02
200MG 10
200MG 20
Y
N
oral
J01AA02
Product
Pack
Reg. Nr.
Reg. Type
Reg. Date
Reg. Valid
Revocation
Company
100MG 10
15/ 179/85-C
NP
200MG 10
200MG 20
15/ 035/02-C
15/ 035/02-C
NP
NP
100MG 10
100MG 20
15/ 073/97-C
15/ 073/97-C
NP
NP
200MG 10
200MG 20
15/ 074/97-C
15/ 074/97-C
NP
NP
Product
Pack
Ex-fact
Wholesale
Net retail
Gr. retail
Company
100MG 10
51
76,86
200MG 10
200MG 20
75,31
0
113,49
100MG 10
100MG 20
55,09
88,8
83,02
133,82
200MG 10
200MG 20
90
96,21
135,63
144,99
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Denmark (5)
X
Product
Pack
Market
Pres.
Dosage
ATC
Company
Product
Pack
Reg. Nr.
Reg. Type
Reg. Date
Reg. Valid
Revocation
Company
28105546915
PI
25-02-2015
28104653810
PI
19-11-2010
28104684910
MRP
13-12-2010
28101410890
NP
14-06-1991
28101410990
NP
14-06-1991
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Hungary (9)
X
Product
Pack
Market
Pres.
Dosage
ATC
Company
100x blister
10x blister
16x blister
200x blister
20x blister
8x blister
N
N
N
N
Y
N
Rx
Rx
Rx
Rx
Rx
Rx
oral
J01AA02
10x blister
N
Rx
oral
J01AA02
10x blister
20x blister
Y
Y
Rx
Rx
oral
J01AA02
10x blister
Y
Rx
oral
J01AA02
100x container
20x blister
30x blister
8x blister
N
N
Y
Y
Rx
Rx
Rx
Rx
oral
J01AA02
16x pp container
Y
Rx
oral
J01AA02
10x blister
30x blister
N
N
Rx
Rx
oral
J01AA02
10x blister
30x blister
N
N
Rx
Rx
oral
J01AA02
60x blister
Y
Rx
oral
J01AA02
Product
Pack
Reg. Nr.
Reg. Type
Reg. Date
Reg. Valid
Revocation
Company
100x blister
10x blister
16x blister
200x blister
20x blister
8x blister
OGYI-T-20573/09
OGYI-T-20573/03
OGYI-T-20573/05
OGYI-T-20573/11
OGYI-T-20573/07
OGYI-T-20573/01
03-06-2008
03-06-2008
03-06-2008
03-06-2008
03-06-2008
03-06-2008
10x blister
OGYI-T-20573/15
03-06-2008
10x blister
20x blister
OGYI-T-04719/01
OGYI-T-04719/02
26-10-1995
26-10-1995
10x blister
OGYI-T-04719/03
26-10-1995
100x container
20x blister
30x blister
8x blister
OGYI-T-03545/02
OGYI-T-03545/04
OGYI-T-03545/03
OGYI-T-03545/01
01-01-1977
01-01-1977
01-01-1977
01-01-1977
16x pp container
OGYI-T-04856/02
04-01-1996
10x blister
30x blister
OGYI-T-04517/02
OGYI-T-04517/01
01-06-1995
01-06-1995
10x blister
30x blister
OGYI-T-04517/04
OGYI-T-04517/03
01-06-1995
01-06-1995
60x blister
OGYI-T-04516/01
Product
Pack
Ex-fact
Wholesale
Net retail
Gr. retail
Company
100x blister
10x blister
16x blister
200x blister
20x blister
8x blister
0
0
0
0
425
0
0
0
0
0
459
0
0
0
0
0
583
0
0
0
0
0
612
0
10x blister
0
0
0
0
10x blister
20x blister
0
450
0
486
0
617
0
648
10x blister
532
572
708
743
100x container
20x blister
30x blister
8x blister
2887
0
637
0
3014,03
0
678,41
0
3617
0
834
0
3798
0
876
0
16x pp container
0
0
0
0
10x blister
30x blister
222
0
239,76
0
304
0
319
0
10x blister
30x blister
0
0
0
0
0
0
0
0
60x blister
1025
1090
1341
1408
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Iceland (3)
X
Product
Pack
Market
Pres.
Dosage
ATC
Company
Y
Y
Y
Rx
Rx
Rx
-
J01AA02
Product
Pack
Reg. Nr.
Reg. Type
Reg. Date
Reg. Valid
Revocation
Company
16-05-2008
16-05-2008
16-05-2008
Product
Pack
Ex-fact
Wholesale
Net retail
Gr. retail
Company
898
1.680
795
898
1.680
795
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Ireland (6)
X
Product
Pack
Reg. Nr.
Reg. Type
Reg. Date
Reg. Valid
Revocation
Company
PA1457/010/002
08-09-1994
PA1457/010/001
08-09-1994
PA0688/042/001
22-07-2010
PA1986/081/001
07-05-1985
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 (7)
X
Product
Pack
Market
Pres.
Dosage
ATC
Company
N10 blister
N8 blister
Rx
Rx
oral
J01AA02
N10 blister
N8 blister
Rx
Rx
oral
J01AA02
N10 blister
Rx
oral
J01AA02
N6 blister
Rx
oral
J01AA02
N10 blister
N20 blister
Rx
Rx
oral
J01AA02
N10 blister
N20 blister
Rx
Rx
oral
J01AA02
N10 blister
Rx
oral
J01AA02
Product
Pack
Reg. Nr.
Reg. Type
Reg. Date
Reg. Valid
Revocation
Company
N10 blister
N8 blister
LT/1/98/0026/002
LT/1/98/0026/001
NP
NP
22-10-1998
22-10-1998
N10 blister
N8 blister
LT/1/98/0026/004
LT/1/98/0026/003
NP
NP
22-10-1998
22-10-1998
N10 blister
LT/1/94/0272/001
NP
05-05-1994
N6 blister
LT/1/95/1850/001
NP
10-05-1995
N10 blister
N20 blister
LT/1/95/1914/001
LT/1/95/1914/002
NP
NP
15-02-1995
15-02-1995
N10 blister
N20 blister
LT/1/95/1914/003
LT/1/95/1914/004
NP
NP
15-02-1995
15-02-1995
N10 blister
LT/1/94/0849/001
NP
07-09-1994
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Malta (8)
X
Product
Pack
Reg. Nr.
Reg. Type
Reg. Date
Reg. Valid
Revocation
Company
MA084/03901
27-11-2006
MA129/00401
03-11-2006
AA1106/00701
15-10-2017
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Poland (7)
X
Product
Pack
Market
Pres.
Dosage
ATC
Company
1 vial 5 ml
10 amp 5 ml
10 vial 5 ml
Lz
Lz
Lz
-
J01AA02
10 tabs
Rp
-
J01AA02
14 caps
28 caps
56 caps
Rp
Rp
Rp
-
J01AA02
10 sachet
16 sachet
2 sachet
4 sachet
8 sachet
Rp
Rp
Rp
Rp
Rp
-
A01AB22
Product
Pack
Reg. Nr.
Reg. Type
Reg. Date
Reg. Valid
Revocation
Company
1 vial 5 ml
10 amp 5 ml
10 vial 5 ml
00762
00762
00762
NP
NP
NP
10 tabs
08882
NP
20-06-2017
14 caps
28 caps
56 caps
18236
18236
18236
MRP
MRP
MRP
10 sachet
16 sachet
2 sachet
4 sachet
8 sachet
22045
22045
22045
22045
22045
DCP
DCP
DCP
DCP
DCP
13-08-2019
13-08-2019
13-08-2019
13-08-2019
13-08-2019
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Romania (2)
X
Product
Pack
Market
Pres.
Dosage
ATC
Company
100 blister Al/PVC x 10 caps ( uz spital
2 blister Al/PVC x 10 caps
-
-
PRF
PRF
-
J01AA02
1 blister PVC/Al x 10 caps
100 blister PVC/Al x 10 caps
-
-
PRF
PRF
-
J01AA02
Product
Pack
Reg. Nr.
Reg. Type
Reg. Date
Reg. Valid
Revocation
Company
100 blister Al/PVC x 10 caps ( uz spital
2 blister Al/PVC x 10 caps
-
-
1 blister PVC/Al x 10 caps
100 blister PVC/Al x 10 caps
-
-
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Slovenia (10)
X
Product
Pack
Market
Pres.
Dosage
ATC
Company
25 tablet 50 mg
-
Rx
oral
J01AA02
50 tabs (2 x 25 tabs blister)
-
Rx
oral
J01AA02
100 caps 100 mg
25 caps 100 mg
6 caps 100 mg
-
-
-
Rx
Rx
Rx
oral
J01AA02
16 tabs (2 x 8 tabs blister)
8 tabs (1 x 8 tabs blister)
N
-
Rx
Rx
oral
J01AA02
10 tabs
-
-
J01AA02
50 tabs
-
-
J01AA02
stekleničko 100 caps
stekleničko 5 kapsul
-
-
Rx
Rx
oral
J01AA02
30 50 mg
-
Rx
oral
J01AA02
Product
Pack
Reg. Nr.
Reg. Type
Reg. Date
Reg. Valid
Revocation
Company
25 tablet 50 mg
-
50 tabs (2 x 25 tabs blister)
-
100 caps 100 mg
25 caps 100 mg
6 caps 100 mg
-
-
-
16 tabs (2 x 8 tabs blister)
8 tabs (1 x 8 tabs blister)
1001-3/2017-12
1001-3/2017-12
NP
NP
16-03-2018
16-03-2018
30 tabs
/
-
22-03-2010
22-03-2015
28 tabs
/
-
22-03-2010
22-03-2015
10 tabs
/
-
28-12-2010
28-12-2015
50 tabs
/
-
28-12-2010
28-12-2015
stekleničko 100 caps
stekleničko 5 kapsul
-
-
Product
Pack
Ex-fact
Wholesale
Net retail
Gr. retail
Company
25 tablet 50 mg
50 tabs (2 x 25 tabs blister)
100 caps 100 mg
25 caps 100 mg
6 caps 100 mg
16 tabs (2 x 8 tabs blister)
8 tabs (1 x 8 tabs blister)
3,21
1,85
stekleničko 100 caps
stekleničko 5 kapsul
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Spain (16)
X
Product
Pack
Market
Pres.
Dosage
ATC
Company
12 caps
14 caps
500 caps
Y
Y
Y
Rx
Rx
Rx
oral
J01AA02
14 grageas
16 grageas
21 grageas
42 grageas
Y
-
Y
Y
Rx
Rx
Rx
Rx
oral
J01AA02
12 tabs
14 tabs
28 tabs
42 tabs
Y
Y
-
Y
Rx
Rx
Rx
Rx
oral
J01AA02
12 caps
30 caps
-
-
Rx
Rx
oral
J01AA02
30 caps
42 caps
Y
Y
Rx
Rx
oral
J01AA02
12 caps
14 caps
Y
Y
Rx
Rx
oral
J01AA02
2 x 260 mg
Y
Rx
periodontal
A01AB22
30 caps
-
Rx
oral
J01AA02
30 caps
42 caps
Y
Y
Rx
Rx
oral
J01AA02
30 caps
42 caps
Y
Y
Rx
Rx
oral
J01AA02
30 caps
Y
Rx
oral
J01AA02
30 caps
42 caps
Y
Y
Rx
Rx
oral
J01AA02
1 bottle of 60 ml
Y
Rx
oral
J01AA02
12 caps
14 caps
Y
Y
Rx
Rx
oral
J01AA02
1 amp of 5 ml
100 amp of 5 ml
Y
Y
Rx
Rx
iv
J01AA02
Product
Pack
Reg. Nr.
Reg. Type
Reg. Date
Reg. Valid
Revocation
Company
12 caps
14 caps
500 caps
48194
48194
48194
01-11-1969
01-11-1969
01-11-1969
14 grageas
16 grageas
21 grageas
42 grageas
47077
47077
47077
47077
01-12-1968
01-12-1968
01-12-1968
01-12-1968
12 tabs
14 tabs
28 tabs
42 tabs
50404
50404
50404
50404
01-09-1972
01-09-1972
01-09-1972
01-09-1972
12 caps
30 caps
48147
48147
01-01-1970
01-01-1970
30 caps
42 caps
59345
59345
01-12-1992
01-12-1992
12 caps
14 caps
47831
47831
01-12-1969
01-12-1969
2 x 260 mg
78353
03-03-2015
30 caps
70306
11-12-2008
28 caps
56 caps
73622
73622
26-07-2011
26-07-2011
30 caps
42 caps
61226
61226
23-12-1999
23-12-1999
30 caps
42 caps
61227
61227
23-12-1999
23-12-1999
30 caps
61230
23-12-1999
30 caps
42 caps
47796
47796
01-01-1970
01-01-1970
1 bottle of 60 ml
46554
01-09-1968
12 caps
14 caps
46406
46406
01-09-1968
01-09-1968
1 amp of 5 ml
100 amp of 5 ml
50521
50521
01-09-1972
01-09-1972
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 (12)
X
Product
Pack
Reg. Nr.
Reg. Type
Reg. Date
Reg. Valid
Revocation
Company
Nationell decentral eller ömsesidig
29-06-2001
31-05-2011
PI
PI
05-10-2009
23-08-2017
31-01-2020
PI
PI
PI
15-08-2018
30-11-2016
29-11-2017
Nationell decentral eller ömsesidig
24-01-2013
Nationell decentral eller ömsesidig
19-03-1993
Nationell decentral eller ömsesidig
19-03-1993
Nationell decentral eller ömsesidig
28-11-2008
PI
13-04-2016
31-01-2018
Nationell decentral eller ömsesidig
16-08-1968
Nationell decentral eller ömsesidig
17-12-1982
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.

Switzerland (14)
X
Product
Pack
Reg. Nr.
Reg. Type
Reg. Date
Reg. Valid
Revocation
Company
44000 3
44000 3
Hauptzulassung
Hauptzulassung
08-07-1981
08-07-1981
14-05-2021
14-05-2021
44000 4
Hauptzulassung
08-07-1981
14-05-2021
65952 1
65952 1
Hauptzulassung
Hauptzulassung
03-09-2015
03-09-2015
65952 2
Hauptzulassung
03-09-2015
42688 1
42688 1
Hauptzulassung
Hauptzulassung
12-03-1980
12-03-1980
50748 1
Hauptzulassung
15-02-1991
16-03-2021
50748 2
Hauptzulassung
15-02-1991
16-03-2021
61686 1
61686 1
Hauptzulassung
Hauptzulassung
15-03-2012
15-03-2012
14-03-2022
14-03-2022
49771 1
49771 1
Hauptzulassung
Hauptzulassung
23-11-1988
23-11-1988
07-01-2022
07-01-2022
49771 2
Hauptzulassung
23-11-1988
07-01-2022
49414 1
Hauptzulassung
23-12-1987
18-12-2021
43416 1
43416 1
Hauptzulassung
Hauptzulassung
14-10-1980
14-10-1980
18-12-2021
18-12-2021
43416 2
Hauptzulassung
14-10-1980
18-12-2021
36829 1
Hauptzulassung
14-01-1972
18-12-2021
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.