Last Updated: June 25, 2026

IBANDRONATE Drug Patent Profile


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Which patents cover Ibandronate, and what generic alternatives are available?

Ibandronate is a drug marketed by Accord Hlthcare, Apotex, Avet Lifesciences, Chemi Spa, Eugia Pharma, Nang Kuang Pharm Co, Pharmobedient, Sun Pharm, Apotex Inc, Aurobindo Pharma, Dr Reddys Labs Ltd, Macleods Pharms Ltd, Orbion Pharms, Sun Pharm Industries, and Watson Labs Teva. and is included in sixteen NDAs.

The generic ingredient in IBANDRONATE 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 Ibandronate

A generic version of IBANDRONATE was approved as ibandronate sodium by APOTEX INC on March 19th, 2012.

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Summary for IBANDRONATE
US Patents:0
Applicants:15
NDAs:16
Drug Prices: Drug price information for IBANDRONATE
DailyMed Link:IBANDRONATE at DailyMed

US Patents and Regulatory Information for IBANDRONATE

Applicant Tradename Generic Name Dosage NDA Approval Date TE Type RLD RS Patent No. Patent Expiration Product Substance Delist Req. Exclusivity Expiration
Accord Hlthcare IBANDRONATE SODIUM ibandronate sodium INJECTABLE;INTRAVENOUS 206058-001 Feb 5, 2016 AP RX No No ⤷  Start Trial ⤷  Start Trial ⤷  Start Trial
Pharmobedient IBANDRONATE SODIUM ibandronate sodium INJECTABLE;INTRAVENOUS 202671-001 Sep 2, 2014 AP RX No No ⤷  Start Trial ⤷  Start Trial ⤷  Start Trial
Chemi Spa IBANDRONATE SODIUM ibandronate sodium INJECTABLE;INTRAVENOUS 202235-001 Sep 2, 2014 AP RX No No ⤷  Start Trial ⤷  Start Trial ⤷  Start Trial
Macleods Pharms Ltd IBANDRONATE SODIUM ibandronate sodium TABLET;ORAL 206887-001 Oct 31, 2017 AB RX No No ⤷  Start Trial ⤷  Start Trial ⤷  Start Trial
Sun Pharm IBANDRONATE SODIUM ibandronate sodium INJECTABLE;INTRAVENOUS 090853-001 Feb 14, 2014 DISCN No No ⤷  Start Trial ⤷  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

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