BONIVA Drug Patent Profile
✉ Email this page to a colleague
When do Boniva patents expire, and when can generic versions of Boniva launch?
Boniva is a drug marketed by Roche and Hoffmann La Roche and is included in two NDAs.
The generic ingredient in BONIVA is ibandronate sodium. There are sixteen drug master file entries for this compound. Ten suppliers are listed for this compound. Additional details are available on the ibandronate sodium profile page.
DrugPatentWatch® Litigation and Generic Entry Outlook for Boniva
A generic version of BONIVA was approved as ibandronate sodium by APOTEX INC on March 19th, 2012.
AI Research Assistant
Questions you can ask:
- What is the 5 year forecast for BONIVA?
- What are the global sales for BONIVA?
- What is Average Wholesale Price for BONIVA?
Summary for BONIVA
US Patents: | 0 |
Applicants: | 2 |
NDAs: | 2 |
Raw Ingredient (Bulk) Api Vendors: | 84 |
Clinical Trials: | 13 |
Patent Applications: | 3,787 |
Drug Prices: | Drug price information for BONIVA |
Patent Litigation and PTAB cases: | See patent lawsuits and PTAB cases for BONIVA |
What excipients (inactive ingredients) are in BONIVA? | BONIVA excipients list |
DailyMed Link: | BONIVA at DailyMed |
Recent Clinical Trials for BONIVA
Identify potential brand extensions & 505(b)(2) entrants
Sponsor | Phase |
---|---|
Hoffmann-La Roche | Phase 3 |
Hoffmann-La Roche | |
M.D. Anderson Cancer Center | Phase 3 |
Paragraph IV (Patent) Challenges for BONIVA
Tradename | Dosage | Ingredient | Strength | NDA | ANDAs Submitted | Submissiondate |
---|---|---|---|---|---|---|
BONIVA | Injection | ibandronate sodium | 1 mg/mL, 3 mL Vial | 021858 | 1 | 2007-08-31 |
BONIVA | Tablets | ibandronate sodium | 2.5 mg | 021455 | 1 | 2007-05-16 |
US Patents and Regulatory Information for BONIVA
Applicant | Tradename | Generic Name | Dosage | NDA | Approval Date | TE | Type | RLD | RS | Patent No. | Patent Expiration | Product | Substance | Delist Req. | Exclusivity Expiration |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
Roche | BONIVA | ibandronate sodium | INJECTABLE;INTRAVENOUS | 021858-001 | Jan 6, 2006 | DISCN | Yes | No | ⤷ Sign Up | ⤷ Sign Up | ⤷ Sign Up | ||||
Hoffmann La Roche | BONIVA | ibandronate sodium | TABLET;ORAL | 021455-001 | May 16, 2003 | DISCN | Yes | No | ⤷ Sign Up | ⤷ Sign Up | ⤷ Sign Up | ||||
Hoffmann La Roche | BONIVA | ibandronate sodium | TABLET;ORAL | 021455-002 | Mar 24, 2005 | DISCN | Yes | No | ⤷ Sign Up | ⤷ Sign Up | ⤷ Sign Up | ||||
>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 BONIVA
Applicant | Tradename | Generic Name | Dosage | NDA | Approval Date | Patent No. | Patent Expiration |
---|---|---|---|---|---|---|---|
Hoffmann La Roche | BONIVA | ibandronate sodium | TABLET;ORAL | 021455-002 | Mar 24, 2005 | ⤷ Sign Up | ⤷ Sign Up |
Hoffmann La Roche | BONIVA | ibandronate sodium | TABLET;ORAL | 021455-002 | Mar 24, 2005 | ⤷ Sign Up | ⤷ Sign Up |
Hoffmann La Roche | BONIVA | ibandronate sodium | TABLET;ORAL | 021455-002 | Mar 24, 2005 | ⤷ Sign Up | ⤷ Sign Up |
Roche | BONIVA | ibandronate sodium | INJECTABLE;INTRAVENOUS | 021858-001 | Jan 6, 2006 | ⤷ Sign Up | ⤷ Sign Up |
>Applicant | >Tradename | >Generic Name | >Dosage | >NDA | >Approval Date | >Patent No. | >Patent Expiration |
International Patents for BONIVA
See the table below for patents covering BONIVA around the world.
Country | Patent Number | Title | Estimated Expiration |
---|---|---|---|
China | 1319015 | ⤷ Sign Up | |
European Patent Office | 1658852 | ⤷ Sign Up | |
Japan | 2015083592 | 骨粗鬆症の治療および予防用のビスホスホン酸 (BISPHOSPHONIC ACID FOR TREATING AND PREVENTING OSTEOPOROSIS) | ⤷ Sign Up |
New Zealand | 556278 | Bisphosphonic acid for the treatment and prevention of osteoperosis | ⤷ Sign Up |
>Country | >Patent Number | >Title | >Estimated Expiration |
Supplementary Protection Certificates for BONIVA
Patent Number | Supplementary Protection Certificate | SPC Country | SPC Expiration | SPC Description |
---|---|---|---|---|
0252504 | 96C0046 | Belgium | ⤷ Sign Up | PRODUCT NAME: DOXORUBICIN HYDROCHLORIDE; REGISTRATION NO/DATE: EU/1/96/011/001 19960624 |
0252504 | C960032 | Netherlands | ⤷ Sign Up | PRODUCT NAME: ACIDUM IBANDRONICUM, DESGEWENST IN DE VORM VAN EEN FARMACOLO- GISCH AANVAARDBAAR ZOUT OF IN DE VORM VAN EEN ESTER MET METHANOL,ETHANOL,2-PROPANOL OF 2-METHYLPROPANOL, OF IN DE VORM VEN EEN HYDRAAT,I.H.B.MONONATRIUM IBANDRONAAT MONOHYDRAAT; REGISTRATION NO/DATE: EU/1/96/012/001 19960625 |
0252504 | SPC/GB96/060 | United Kingdom | ⤷ Sign Up | PRODUCT NAME: IBANDRONIC ACID ((1-HYDROXY-3-(METHYLPENTYLAMINO) - PROPYLIDINE)-DIPHOSPHONIC ACID); REGISTERED: UK EU/1/96/012/001 19960625 |
>Patent Number | >Supplementary Protection Certificate | >SPC Country | >SPC Expiration | >SPC Description |