IP Library Granted Patent US 11,878,022
Granted Patent B2
US 11,878,022 · App. 18/053,197 · Granted Jan 23, 2024

Hydrochlorothiazide compositions

Inventors: Muthusamy Shanmugam (East Windsor, NJ); Subramaniam Arunkumar (East Windsor, NJ)
Assignee: Novitium Pharma LLC
A61K31/549A61K9/0056A61K9/0095A61K47/02A61K47/12A61K47/26A61K47/36
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Quick Facts
Patent No.
US 11,878,022
App. No.
18/053,197
Granted
Jan 23, 2024
Kind
B2
Abstract

Disclosed herein is a powder for oral suspension and a reconstituted product thereof comprising highly pure hydrochlorothiazide, which is useful for treating hypertension and edema.

Claims (24)

1. A powder for oral suspension for oral administration, comprising

about 3% w/w to about 5% w/w of hydrochlorothiazide;

at least one thickening agent; and

at least one pharmaceutically acceptable excipient;

wherein the powder for oral suspension composition in 5 mL of water has a pH of from about 3.5 to about 5.5.

2. The powder of claim 1 comprising about 3.5% w/w to about 4.4% w/w of hydrochlorothiazide.

3. The powder of claim 1 comprising about 4.2% w/w of hydrochlorothiazide.

4. The powder of claim 1 having a water content of not more than about 0.8% w/w.

5. The powder of claim 1 , wherein the at least one thickening agent is selected from hydrocolloid gum, cellulosic derivative, a polysaccharide, alginate, acrylic acid copolymer, polyvinylpyrrolidone, aluminium magnesium silicate, and a combination thereof.

6. The powder of claim 1 , wherein the amount of the at least one thickening agent is in an amount of from about 0.4% w/w to about 5% w/w.

7. The powder of claim 1 , wherein the at least one thickening agent comprises xanthan gum in an amount of from about 0.4% w/w to about 2.5% w/w.

8. The powder of claim 1 , wherein the at least one pharmaceutically acceptable excipient comprises a preservative and a sweetener.

9. The powder of claim 1 , wherein the at least one pharmaceutically acceptable excipient comprises a preservative selected from the group consisting of sodium benzoate, benzoic acid, potassium sorbate, paraben, methylparaben, ethylparaben, propylparaben, butylparaben, isobutylparaben, benzyl alcohol, boric acid, calcium acetate, bentonite, cetrimide, chlorhexidine, cetylpyridinium chloride, cresol, chlorbutanol, magnesium tri silicate, and a combination thereof.

10. The powder of claim 1 , wherein the at least one pharmaceutically acceptable excipient comprises a preservative selected from the group consisting of sodium benzoate, benzoic acid, potassium sorbate, paraben, methylparaben, ethylparaben, propylparaben, butylparaben, isobutylparaben, benzyl alcohol, boric acid, calcium acetate, bentonite, cetrimide, chlorhexidine, cetylpyridinium chloride, cresol, chlorbutanol, magnesium trisilicate, and combination thereof in an amount of from about 0.01% w/w to about 5% w/w.

11. The powder of claim 1 , wherein the at least one pharmaceutically acceptable excipient comprises a sweetener selected from the group consisting of sucralose, maltilol, liquid glucose, magnasweet 110, magnasweet 180, saccharin sodium, xylitol, sorbitan monoleate, sorbitol, sucrose, aspartame, acesulfame potassium, and a combination thereof.

12. The powder of claim 1 , wherein the at least one pharmaceutically acceptable excipient comprises a sweetener selected from the group consisting of sucralose, maltilol, liquid glucose, magnasweet 110, magnasweet 180, saccharin sodium, xylitol, sorbitan monoleate, sorbitol, sucrose, aspartame, acesulfame potassium, and a combination thereof in an amount of from about 0.1% w/w to about 96% w/w.

13. The powder of claim 1 , wherein the at least one pharmaceutically acceptable excipient comprises a sweetener selected from the group consisting of sucralose, sucrose, and a combination thereof in an amount of from about 90% w/w to about 96% w/w.

14. The powder of claim 1 , wherein the at least one pharmaceutically acceptable excipient comprises a pH modifier selected from group consisting of citric acid, fumaric acid, tartaric acid, malic acid, sodium phosphate monobasic, potassium phosphate, maleic acid, lactic acid, hydrochloric acid, phosphoric acid, and a combination thereof.

15. The powder of claim 1 , wherein the at least one pharmaceutically acceptable excipient comprises a pH modifier selected from group consisting of citric acid, fumaric acid, tartaric acid, malic acid, sodium phosphate monobasic, potassium phosphate, maleic acid, lactic acid, hydrochloric acid, phosphoric acid, and a combination thereof in an amount of from about w/w to about 1.2% w/w.

16. The powder of claim 1 , having a salamide impurity content not more than 1.0% for at least about 6-months when stored at 25±2° C. and 60±5% relative humidity, 40° C. and 75% relative humidity and a salamide impurity content not more than 1.0% for at least about 6-months when stored at 25±2° C. and 60±5% relative humidity after reconstitution.

17. An oral liquid suspension comprising the powder of claim 1 and a pharmaceutically acceptable carrier comprising water.

18. The oral liquid suspension of claim 17 having a volume of from about 50 mL to about 150 mL.

19. A method of treating edema and hypertension comprising administering to a patient in need thereof a therapeutically effective amount of the oral liquid suspension of claim 17 .

20. The method of claim 19 , wherein administration of the oral liquid suspension to the human patient provides a geometric least squares mean for C max of from about 200 ng/mL to about 450 ng/mL, a geometric least squares mean for AUC 0-∞ of from about 1800 ng•hr/mL to about 2900 ng•hr/mL, or a combination thereof.

Assignments (2)
SECURITY INTEREST Recorded Aug 14, 2024
From: NOVITIUM PHARMA LLC
To: JPMORGAN CHASE BANK, N.A., AS ADMINISTRATIVE AGENT
Reel/Frame 068277/0142 →
ASSIGNMENT OF ASSIGNOR'S INTEREST Recorded Jan 10, 2023
From: SHANMUGAM, MUTHUSAMY; ARUNKUMAR, SUBRAMANIAM
To: NOVITIUM PHARMA LLC
Reel/Frame 062321/0423 →
Priority Claims (1)
IN 202041053842 · Dec 10, 2020 · national
Continuity (2)
Continuation In Part 17546175 · Dec 9, 2021
Related Publication 20230111273A1 · Apr 13, 2023