You’re using a public version of DrugPatentWatch with 5 free searches available | Register to unlock more free searches. CREATE FREE ACCOUNT

Last Updated: April 25, 2024

Claims for Patent: 9,693,979


✉ Email this page to a colleague

« Back to Dashboard


Summary for Patent: 9,693,979
Title:Liquid dosage forms of sodium naproxen
Abstract: Described herein are oral pharmaceutical compositions comprising liquid dosage forms of sodium naproxen in soft gel capsules. In one embodiment, the pharmaceutical composition comprises sodium naproxen, 0.2-1.0 mole equivalents of a de-ionizing agent per mole of naproxen, polyethylene glycol, and one or more solubilizers such as propylene glycol, polyvinyl pyrrolidone or a combination thereof.
Inventor(s): Chidambaram; Nachiappan (Sandy, UT), Fatmi; Aqeel A (High Point, NC)
Assignee: Banner Life Sciences LLC (High Point, NC)
Application Number:15/159,972
Patent Litigation and PTAB cases: See patent lawsuits and PTAB cases for patent 9,693,979
Patent Claims: 1. A pharmaceutical composition comprising a soft gelatin capsule encapsulating a liquid matrix comprising: (a) naproxen sodium; (b) about 5% lactic acid by weight of the matrix; (c) one or more polyethylene glycols; and (d) one or more solubilizers comprising polyvinylpyrrolidone, propylene glycol, or a combination thereof.

2. The composition of claim 1, wherein the polyethylene glycol comprises from about 10% to about 80% by weight of the matrix.

3. The composition of claim 1, wherein the polyethylene glycol comprises one or more polyethylene glycols with a molecular weight between 300 and 1500.

4. The composition of claim 1, wherein the polyethylene glycol comprises polyethylene glycol 600.

5. The composition of claim 1, wherein the solubilizer comprises from about 1% to 10% by weight of the matrix.

6. The composition of claim 1, wherein the solubilizer comprises about 2% polyvinylpyrrolidone and about 2% propylene glycol by weight of the matrix.

7. The composition of claim 1, further comprising one or more excipients comprising plasticizers, crystallization inhibitors, wetting agents, bulk filling agents, bioavailability enhancers, solvents, dyes, preservatives, surfactants, or combinations thereof.

8. A pharmaceutical composition comprising a soft gelatin capsule encapsulating a liquid matrix comprising: (a) about 25% naproxen sodium by weight of the matrix; (b) about 5% lactic acid by weight of the matrix; (c) about 10% to about 80% of polyethylene glycol 600 by weight of the matrix; and (d) about 1% to about 10% of one or more solubilizers comprising polyvinylpyrrolidone, propylene glycol, or a combination thereof by weight of the matrix.

9. The composition of claim 8, wherein the solubilizer comprises propylene glycol and polyvinyl pyrrolidone.

10. The composition of claim 8, wherein the matrix comprises a mole ratio of lactic acid to naproxen sodium of about 0.6.

11. The composition of claim 8, wherein the solubilizer comprises about 2% polyvinylpyrrolidone and about 2% propylene glycol by weight of the matrix.

12. The composition of claim 8, wherein the matrix further comprises one or more excipients selected from plasticizers, crystallization inhibitors, wetting agents, bulk filling agents, bioavailability enhancers, solvents, dyes, preservatives, surfactants, or combinations thereof.

13. The composition of claim 8, wherein the matrix comprises a pH from about 2.5 to about 7.5.

14. The composition of claim 8, wherein the soft gelatin capsule comprises: (a) gelatin; (b) plasticizer; and (c) purified water.

15. A method for making the pharmaceutical composition of claim 8, the method comprising: (a) mixing together the components of 10(a) to 10(d) to form a mixture; and (b) encapsulating the mixture in a soft gelatin capsule using rotary die encapsulation.

16. An oral dosage form produced by the method of claim 15.

17. A pharmaceutical composition comprising a soft gelatin capsule encapsulating a liquid matrix comprising: (a) about 25% naproxen sodium by weight of the matrix; (b) about 5% lactic acid by weight of the matrix; (c) quantum sufficit (q.s.) of polyethylene glycol 600; and (d) about 1% to about 10% of one or more solubilizers comprising polyvinylpyrrolidone, propylene glycol, or a combination thereof by weight of the matrix.

18. The composition of claim 17, wherein the solubilizer comprises about 2% polyvinylpyrrolidone and about 2% propylene glycol by weight of the matrix.

19. The composition of claim 17, wherein the matrix comprises a mole ratio of lactic acid to naproxen sodium of about 0.6.

Make Better Decisions: Try a trial or see plans & pricing

Drugs may be covered by multiple patents or regulatory protections. All trademarks and applicant names are the property of their respective owners or licensors. Although great care is taken in the proper and correct provision of this service, thinkBiotech LLC does not accept any responsibility for possible consequences of errors or omissions in the provided data. The data presented herein is for information purposes only. There is no warranty that the data contained herein is error free. thinkBiotech performs no independent verification of facts as provided by public sources nor are attempts made to provide legal or investing advice. Any reliance on data provided herein is done solely at the discretion of the user. Users of this service are advised to seek professional advice and independent confirmation before considering acting on any of the provided information. thinkBiotech LLC reserves the right to amend, extend or withdraw any part or all of the offered service without notice.