Pradaxa is owned by Boehringer Ingelheim.
Pradaxa contains Dabigatran Etexilate Mesylate.
Pradaxa has a total of 9 drug patents out of which 1 drug patent has expired.
Expired drug patents of Pradaxa are:
Pradaxa was authorised for market use on 19 October, 2010.
Pradaxa is available in capsule;oral dosage forms.
Pradaxa can be used as method of reversing the anticoagulant effect of dabigatran using idarucizumab.
The generics of Pradaxa are possible to be released after 20 July, 2031.
Patent Number | Company | Patent Title | Patent Expiry | Activity Alert |
---|---|---|---|---|
These patents protects the active chemical substance. Only patent owner can launch products that use this active substance. | ||||
US7932273 | BOEHRINGER INGELHEIM | 3-[(2-{[4-(hexyloxycarbonylaminoiminomethyl) phenylamino]methyl}-1-methyl-1H-benzimidazol-5-carbonyl)pyridin-2-ylamino]propionic acid ethylester methansulfonate and its use as a medicament |
Sep, 2025
(2 years from now) | |
These patents focus on the other aspects of the active substance like dosage, mode of administration (oral, tablet, capsules, liquids etc). | ||||
US6087380 (Pediatric) | BOEHRINGER INGELHEIM | Disubstituted bicyclic heterocycles, the preparations and the use thereof as pharmaceutical compositions |
Jun, 2022
(11 months ago) | |
US9925174 | BOEHRINGER INGELHEIM | Administration form for the oral application of 3-[(2-{[4-(hexyloxycarbonyl-amino-imino-methyl)-phenylamino]-methyl}-1-methyl-1 H-benzimidazol acid ethyl ester and the salts thereof |
Jun, 2023
(12 days from now) | |
US9925174 (Pediatric) | BOEHRINGER INGELHEIM | Administration form for the oral application of 3-[(2-{[4-(hexyloxycarbonyl-amino-imino-methyl)-phenylamino]-methyl}-1-methyl-1 H-benzimidazol acid ethyl ester and the salts thereof |
Dec, 2023
(6 months from now) | |
US7932273 (Pediatric) | BOEHRINGER INGELHEIM | 3-[(2-{[4-(hexyloxycarbonylaminoiminomethyl) phenylamino]methyl}-1-methyl-1H-benzimidazol-5-carbonyl)pyridin-2-ylamino]propionic acid ethylester methansulfonate and its use as a medicament |
Mar, 2026
(2 years from now) | |
US7866474 | BOEHRINGER INGELHEIM | Film container |
Aug, 2027
(4 years from now) | |
US7866474 (Pediatric) | BOEHRINGER INGELHEIM | Film container |
Mar, 2028
(4 years from now) | |
US9034822 | BOEHRINGER INGELHEIM | Methods of using antibodies during anticoagulant therapy of dabigatran and/or related compounds |
Jan, 2031
(7 years from now) | |
US9034822 (Pediatric) | BOEHRINGER INGELHEIM | Methods of using antibodies during anticoagulant therapy of dabigatran and/or related compounds |
Jul, 2031
(8 years from now) |
Exclusivity | Exclusivity Expiration |
---|---|
New Indication (I) | Jun 21, 2024 |
Pediatric Exclusivity (PED) | Dec 21, 2024 |
Drugs and Companies using DABIGATRAN ETEXILATE MESYLATE ingredient
Market Authorisation Date: 19 October, 2010
Treatment: Method of reversing the anticoagulant effect of dabigatran using idarucizumab
Dosage: CAPSULE;ORAL
16
United States
13
European Union
8
Norway
8
Japan
7
Germany
6
China
6
New Zealand
6
Korea, Republic of
5
Spain
5
Denmark
5
Poland
5
Canada
5
Ukraine
5
Argentina
5
Cyprus
5
Israel
5
Portugal
5
Australia
5
Slovenia
4
Uruguay
4
Hong Kong
4
Austria
4
Malaysia
4
Brazil
4
EA
4
Croatia
4
Taiwan
4
Mexico
4
Ecuador
4
South Africa
3
Singapore
3
ME
3
Peru
3
Colombia
3
Luxembourg
2
RS
2
Yugoslavia
2
Chile
2
Lithuania
2
Hungary
1
Morocco
1
Georgia
1
Netherlands
1
Tunisia
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