The patent badge is an abbreviated version of the USPTO patent document. The patent badge does contain a link to the full patent document.

The patent badge is an abbreviated version of the USPTO patent document. The patent badge covers the following: Patent number, Date patent was issued, Date patent was filed, Title of the patent, Applicant, Inventor, Assignee, Attorney firm, Primary examiner, Assistant examiner, CPCs, and Abstract. The patent badge does contain a link to the full patent document (in Adobe Acrobat format, aka pdf). To download or print any patent click here.

Date of Patent:
Jan. 12, 2021

Filed:

Jul. 05, 2017
Applicant:

Jubilant Generics Limited, Uttar Pradesh, IN;

Inventors:

Pankaj Soni, Noida, IN;

Premchand Dalichandji Nakhat, Noida, IN;

Ganesh Vinayak Gat, Noida, IN;

Kamal S. Mehta, Noida, IN;

Dinesh Kumar, Noida, IN;

Vikas Bali, Noida, IN;

Attorneys:
Primary Examiner:
Int. Cl.
CPC ...
A61K 9/00 (2006.01); A61K 9/20 (2006.01); A61P 7/00 (2006.01); A61K 31/4196 (2006.01); A61K 9/28 (2006.01);
U.S. Cl.
CPC ...
A61K 9/0056 (2013.01); A61K 9/2013 (2013.01); A61K 9/2018 (2013.01); A61K 9/2027 (2013.01); A61K 9/2031 (2013.01); A61K 9/2054 (2013.01); A61K 9/2095 (2013.01); A61K 9/288 (2013.01); A61K 9/2893 (2013.01); A61K 31/4196 (2013.01); A61P 7/00 (2018.01);
Abstract

The present invention relates to a stable, immediate release solid oral pharmaceutical compositions comprising iron chelating agents like Deferasirox and at least one pharmaceutical acceptable excipient wherein the composition is free of glidant. Prior art discloses various technical challenges and suggest restrictive and complex solutions for the development of immediate release dosage forms of Deferasirox such as utilizing a large number of excipients or non-conventional formulation techniques. The glidant free immediate release solid oral pharmaceutical composition of Deferasirox, prepared as per present invention exhibited desirable technical attributes like pharmaceutical stability, flow properties and comparable dissolution, bioequivalence against reference listed drug.


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