Alendronate Sodium Patent Expiration

Alendronate Sodium was first introduced by Organon Llc A Sub Of Organon And Co in its drug Fosamax on Sep 29, 1995. Another drug containing Alendronate Sodium is Binosto. 19 different companies have introduced drugs containing Alendronate Sodium.


Alendronate Sodium Patents

Given below is the list of patents protecting Alendronate Sodium, along with the drug name that holds that patent and the company name owning that drug.

Drug Used in Drug Patent Number Drug Patent Title Drug Patent Expiry Drug Owner
Binosto US7488496 Effervescent compositions comprising bisphosphonates and methods related thereto Aug 11, 2023

(Expired)

Radius
Binosto US7964212 Effervescent compositions comprising phosphonates and methods related thereto Mar 06, 2023

(Expired)

Radius
Binosto US9592195 Stable effervescent bisphosphonate formulations with rapid solubilization characteristics Dec 05, 2031 Radius
Fosamax US5358941 Dry mix formulation for bisphosphonic acids with lactose Dec 02, 2012

(Expired)

Organon
Fosamax US5358941

(Pediatric)

Dry mix formulation for bisphosphonic acids with lactose Jun 02, 2013

(Expired)

Organon
Fosamax US5462932 Oral liquid alendronate formulations May 17, 2014

(Expired)

Merck
Fosamax US5462932

(Pediatric)

Oral liquid alendronate formulations Nov 17, 2014

(Expired)

Merck
Fosamax US5681590 Dry mix formulation for bisphosphonic acids Dec 02, 2012

(Expired)

Organon
Fosamax US5681590

(Pediatric)

Dry mix formulation for bisphosphonic acids Jun 02, 2013

(Expired)

Organon
Fosamax US5994329 Method for inhibiting bone resorption Jul 17, 2018

(Expired)

Merck
Fosamax US5994329

(Pediatric)

Method for inhibiting bone resorption Jan 17, 2019

(Expired)

Merck
Fosamax US6015801 Method for inhibiting bone resorption Jul 17, 2018

(Expired)

Merck
Fosamax US6015801

(Pediatric)

Method for inhibiting bone resorption Jan 17, 2019

(Expired)

Merck
Fosamax US6090410 Dry mix formulation for bisphosphonic acids Dec 02, 2012

(Expired)

Organon
Fosamax US6090410

(Pediatric)

Dry mix formulation for bisphosphonic acids Jun 02, 2013

(Expired)

Organon
Fosamax US6194004 Dry mix formulation for bisphosphonic acids Dec 02, 2012

(Expired)

Organon
Fosamax US6194004

(Pediatric)

Dry mix formulation for bisphosphonic acids Jun 02, 2013

(Expired)

Organon
Fosamax US6225294 Method for inhibiting bone resorption Jul 17, 2018

(Expired)

Merck
Fosamax US6225294

(Pediatric)

Method for inhibiting bone resorption Jan 17, 2019

(Expired)

Merck


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Alendronate Sodium Generics

Several generic applications have been filed for Alendronate Sodium. The first generic version for Alendronate Sodium was by Impax Laboratories Inc and was approved on Feb 6, 2008. And the latest generic version is by Ipca Laboratories Ltd and was approved on Jun 4, 2024.

Given below is the list of companies who have filed for Alendronate Sodium generic.


1. MYLAN

Mylan Pharmaceuticals Inc has filed for 2 different strengths of generic version for Alendronate Sodium. Given below are the details of the strengths of this generic introduced by Mylan.

Strength Dosage Form Availability Application Pathway TE code Launch Date
EQ 35MG BASE tablet Discontinued ORAL N/A Aug 4, 2008
EQ 70MG BASE tablet Discontinued ORAL N/A Aug 4, 2008


2. CIPLA

Cipla Ltd has filed for 5 different strengths of generic version for Alendronate Sodium. Given below are the details of the strengths of this generic introduced by Cipla.

Strength Dosage Form Availability Application Pathway TE code Launch Date
EQ 5MG BASE tablet Prescription ORAL AB Aug 4, 2008
EQ 10MG BASE tablet Prescription ORAL AB Aug 4, 2008
EQ 35MG BASE tablet Prescription ORAL AB Aug 4, 2008
EQ 40MG BASE tablet Prescription ORAL AB Aug 4, 2008
EQ 70MG BASE tablet Prescription ORAL AB Aug 4, 2008


3. RISING

Rising Pharma Holding Inc has filed for 4 different strengths of generic version for Alendronate Sodium. Given below are the details of the strengths of this generic introduced by Rising.

Strength Dosage Form Availability Application Pathway TE code Launch Date
EQ 35MG BASE tablet Discontinued ORAL N/A Aug 4, 2008
EQ 70MG BASE tablet Discontinued ORAL N/A Aug 4, 2008
EQ 5MG BASE tablet Discontinued ORAL N/A Aug 4, 2008
EQ 10MG BASE tablet Discontinued ORAL N/A Aug 4, 2008


4. CHARTWELL RX

Chartwell Rx Sciences Llc has filed for 5 different strengths of generic version for Alendronate Sodium. Given below are the details of the strengths of this generic introduced by Chartwell Rx.

Strength Dosage Form Availability Application Pathway TE code Launch Date
EQ 35MG BASE tablet Discontinued ORAL N/A Apr 22, 2009
EQ 70MG BASE tablet Discontinued ORAL N/A Apr 22, 2009
EQ 5MG BASE tablet Discontinued ORAL N/A Apr 22, 2009
EQ 10MG BASE tablet Discontinued ORAL N/A Apr 22, 2009
EQ 40MG BASE tablet Discontinued ORAL N/A Apr 22, 2009


5. DR REDDYS LABS LTD

Dr Reddys Laboratories Ltd has filed for 2 different strengths of generic version for Alendronate Sodium. Given below are the details of the strengths of this generic introduced by Dr Reddys Labs Ltd.

Strength Dosage Form Availability Application Pathway TE code Launch Date
EQ 5MG BASE tablet Prescription ORAL AB Aug 4, 2008
EQ 10MG BASE tablet Prescription ORAL AB Aug 4, 2008


6. WATSON LABS

Watson Laboratories Inc has filed for 3 different strengths of generic version for Alendronate Sodium. Given below are the details of the strengths of this generic introduced by Watson Labs.

Strength Dosage Form Availability Application Pathway TE code Launch Date
EQ 35MG BASE tablet Prescription ORAL AB Aug 4, 2008
EQ 40MG BASE tablet Prescription ORAL AB Aug 4, 2008
EQ 70MG BASE tablet Prescription ORAL AB Aug 4, 2008


7. TEVA PHARMS

Teva Pharmaceuticals Usa has filed for 2 different strengths of generic version for Alendronate Sodium. Given below are the details of the strengths of this generic introduced by Teva Pharms.

Strength Dosage Form Availability Application Pathway TE code Launch Date
EQ 70MG BASE tablet Discontinued ORAL N/A Feb 6, 2008
EQ 35MG BASE tablet Discontinued ORAL N/A Aug 4, 2008


8. HANGZHOU BINJIANG

Hangzhou Minsheng Binjiang Pharmaceutical Co Ltd has filed for 4 different strengths of generic version for Alendronate Sodium. Given below are the details of the strengths of this generic introduced by Hangzhou Binjiang.

Strength Dosage Form Availability Application Pathway TE code Launch Date
EQ 10MG BASE tablet Prescription ORAL AB Sep 24, 2009
EQ 5MG BASE tablet Prescription ORAL AB Sep 24, 2009
EQ 35MG BASE tablet Prescription ORAL AB Sep 24, 2009
EQ 70MG BASE tablet Prescription ORAL AB Sep 24, 2009


9. HIKMA

Hikma Pharmaceuticals Usa Inc has filed for 1 generic for Alendronate Sodium. Given below are the details of the strengths of this generic introduced by Hikma.

Strength Dosage Form Availability Application Pathway TE code Launch Date
EQ 70MG BASE/75ML

(reference standard)

solution Prescription ORAL AA Feb 25, 2013


10. AUROBINDO PHARMA

Aurobindo Pharma Ltd has filed for 3 different strengths of generic version for Alendronate Sodium. Given below are the details of the strengths of this generic introduced by Aurobindo Pharma.

Strength Dosage Form Availability Application Pathway TE code Launch Date
EQ 10MG BASE tablet Prescription ORAL AB Aug 4, 2008
EQ 35MG BASE tablet Prescription ORAL AB Aug 4, 2008
EQ 70MG BASE tablet Prescription ORAL AB Aug 4, 2008


11. SUN PHARM

Sun Pharmaceutical Industries Ltd has filed for 4 different strengths of generic version for Alendronate Sodium. Given below are the details of the strengths of this generic introduced by Sun Pharm.

Strength Dosage Form Availability Application Pathway TE code Launch Date
EQ 35MG BASE tablet Prescription ORAL AB Sep 10, 2008
EQ 10MG BASE tablet Prescription ORAL AB Sep 10, 2008
EQ 70MG BASE tablet Prescription ORAL AB Sep 10, 2008
EQ 5MG BASE tablet Prescription ORAL AB Sep 10, 2008


12. IMPAX LABS INC

Impax Laboratories Inc has filed for 5 different strengths of generic version for Alendronate Sodium. Given below are the details of the strengths of this generic introduced by Impax Labs Inc.

Strength Dosage Form Availability Application Pathway TE code Launch Date
EQ 5MG BASE tablet Discontinued ORAL N/A Feb 6, 2008
EQ 10MG BASE tablet Discontinued ORAL N/A Feb 6, 2008
EQ 35MG BASE tablet Discontinued ORAL N/A Feb 6, 2008
EQ 40MG BASE tablet Discontinued ORAL N/A Feb 6, 2008
EQ 70MG BASE tablet Discontinued ORAL N/A Feb 6, 2008


13. JUBILANT CADISTA

Jubilant Cadista Pharmaceuticals Inc has filed for 4 different strengths of generic version for Alendronate Sodium. Given below are the details of the strengths of this generic introduced by Jubilant Cadista.

Strength Dosage Form Availability Application Pathway TE code Launch Date
EQ 35MG BASE tablet Discontinued ORAL N/A Feb 18, 2010
EQ 70MG BASE tablet Discontinued ORAL N/A Feb 18, 2010
EQ 5MG BASE tablet Discontinued ORAL N/A Feb 18, 2010
EQ 10MG BASE tablet Discontinued ORAL N/A Feb 18, 2010


14. IPCA LABS LTD

Ipca Laboratories Ltd has filed for 4 different strengths of generic version for Alendronate Sodium. Given below are the details of the strengths of this generic introduced by Ipca Labs Ltd.

Strength Dosage Form Availability Application Pathway TE code Launch Date
EQ 10MG BASE tablet Prescription ORAL AB Jun 4, 2024
EQ 40MG BASE tablet Prescription ORAL AB Jun 4, 2024
EQ 35MG BASE tablet Prescription ORAL AB Jun 4, 2024
EQ 70MG BASE tablet Prescription ORAL AB Jun 4, 2024


15. APOTEX

Apotex Inc has filed for 4 different strengths of generic version for Alendronate Sodium. Given below are the details of the strengths of this generic introduced by Apotex.

Strength Dosage Form Availability Application Pathway TE code Launch Date
EQ 5MG BASE tablet Prescription ORAL AB Aug 4, 2008
EQ 10MG BASE tablet Prescription ORAL AB Aug 4, 2008
EQ 35MG BASE tablet Prescription ORAL AB Aug 4, 2008
EQ 70MG BASE tablet Prescription ORAL AB Aug 4, 2008


16. NOVITIUM PHARMA

Novitium Pharma Llc has filed for 1 generic for Alendronate Sodium. Given below are the details of the strengths of this generic introduced by Novitium Pharma.

Strength Dosage Form Availability Application Pathway TE code Launch Date
EQ 70MG BASE/75ML solution Prescription ORAL AA May 11, 2023