Pharmobedient Company Profile
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What is the competitive landscape for PHARMOBEDIENT
PHARMOBEDIENT has three hundred and twenty-seven approved drugs.
There is one US patent protecting PHARMOBEDIENT drugs. There is one tentative approval on PHARMOBEDIENT drugs.
There are twenty-one patent family members on PHARMOBEDIENT drugs in sixteen countries and six hundred and eighty-six supplementary protection certificates in nineteen countries.
Summary for Pharmobedient
| International Patents: | 21 |
| US Patents: | 1 |
| Tradenames: | 255 |
| Ingredients: | 243 |
| NDAs: | 327 |
Drugs and US Patents for Pharmobedient
| Applicant | Tradename | Generic Name | Dosage | NDA | Approval Date | TE | Type | RLD | RS | Patent No. | Patent Expiration | Product | Substance | Delist Req. | Exclusivity Expiration |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| Pharmobedient | BENDAMUSTINE HYDROCHLORIDE | bendamustine hydrochloride | POWDER;INTRAVENOUS | 204104-001 | Apr 28, 2023 | DISCN | No | No | ⤷ Start Trial | ⤷ Start Trial | |||||
| Pharmobedient | FLUOXETINE HYDROCHLORIDE | fluoxetine hydrochloride | CAPSULE;ORAL | 075207-002 | Jan 30, 2002 | DISCN | No | No | ⤷ Start Trial | ⤷ Start Trial | |||||
| Pharmobedient | CLOMIPRAMINE HYDROCHLORIDE | clomipramine hydrochloride | CAPSULE;ORAL | 074947-003 | Apr 30, 1998 | DISCN | No | No | ⤷ Start Trial | ⤷ Start Trial | |||||
| >Applicant | >Tradename | >Generic Name | >Dosage | >NDA | >Approval Date | >TE | >Type | >RLD | >RS | >Patent No. | >Patent Expiration | >Product | >Substance | >Delist Req. | >Exclusivity Expiration |
Expired US Patents for Pharmobedient
| Applicant | Tradename | Generic Name | Dosage | NDA | Approval Date | Patent No. | Patent Expiration |
|---|---|---|---|---|---|---|---|
| Pharmobedient | OLUX E | clobetasol propionate | AEROSOL, FOAM;TOPICAL | 022013-001 | Jan 12, 2007 | 6,730,288 | ⤷ Start Trial |
| Pharmobedient | DEMADEX | torsemide | TABLET;ORAL | 020136-002 | Aug 23, 1993 | 4,018,929 | ⤷ Start Trial |
| Pharmobedient | DEMADEX | torsemide | TABLET;ORAL | 020136-001 | Aug 23, 1993 | RE34672 | ⤷ Start Trial |
| >Applicant | >Tradename | >Generic Name | >Dosage | >NDA | >Approval Date | >Patent No. | >Patent Expiration |
Paragraph IV (Patent) Challenges for PHARMOBEDIENT drugs
| Drugname | Dosage | Strength | Tradename | Submissiondate |
|---|---|---|---|---|
| ➤ Subscribe | Foam | 0.12% | ➤ Subscribe | 2007-08-10 |
| ➤ Subscribe | Delayed-release Tablets | 20 mg | ➤ Subscribe | 2015-06-03 |
| ➤ Subscribe | Topical Foam | 0.05% | ➤ Subscribe | 2005-06-27 |
| ➤ Subscribe | Inhalation Solution | 0.021% and 0.042% | ➤ Subscribe | 2005-10-19 |
International Patents for Pharmobedient Drugs
| Country | Patent Number | Estimated Expiration |
|---|---|---|
| Japan | 4972553 | ⤷ Start Trial |
| World Intellectual Property Organization (WIPO) | 2006024095 | ⤷ Start Trial |
| Brazil | PI0514806 | ⤷ Start Trial |
| >Country | >Patent Number | >Estimated Expiration |
Supplementary Protection Certificates for Pharmobedient Drugs
| Patent Number | Supplementary Protection Certificate | SPC Country | SPC Expiration | SPC Description |
|---|---|---|---|---|
| 0780390 | PA2004012 | Lithuania | ⤷ Start Trial | PRODUCT NAME: MOXIFLOXACINI HYDROCHLORIDUM (1-CIKLOPROPIL-6-FLUOR-__ 1,4-DIHIDRO-8-METOKSI-7-[(4AS, 7AS)-OKTAHIDRO-6H-PIROLO[3,4-B]PIRIDIN_-6-IL]-4-OKSO-3-CHINOLINKARBOKSIRûGðTIES HIDROCHLORIDAS) |
| 0240228 | 2000C/015 | Belgium | ⤷ Start Trial | PRODUCT NAME: QUETIAPINE FUMARAT (EQUIV. MET 25MG QUETIAPINE BASE); REGISTRATION NO/DATE: 624 S 309 F 3 20000207; FIRST REGISTRATION: GB PL 12619/0113 19970731 |
| 0299602 | SPC/GB96/040 | United Kingdom | ⤷ Start Trial | PRODUCT NAME: ROPINIROLE, OR A PHARMACEUTICALLY ACCEPTABLE SALT THEREOF, IN PARTICULAR THE HYDROCHLORIDE SALT; REGISTERED: UK 10592/0085 19960702 |
| >Patent Number | >Supplementary Protection Certificate | >SPC Country | >SPC Expiration | >SPC Description |
Similar Applicant Names
Here is a list of applicants with similar names.

