IP Library Granted Patent US 10,159,647
Granted Patent B2
US 10,159,647 · App. 14/916,613 · Granted Dec 25, 2018

Tablet comprising crospovidone

Inventor: Abraham Cornelis Lardée (Echt, NL)
Assignee: DSM Sinochem Pharmaceuticals Netherlands B.V.
A61K9/2027A61K9/0095A61K9/2013A61K9/2095A61K31/424A61K31/43
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Quick Facts
Patent No.
US 10,159,647
App. No.
14/916,613
Granted
Dec 25, 2018
Kind
B2
Abstract

The present invention relates to a dispersible tablet comprising crospovidone, notably a tablet comprising crospovidone and a β-lactam antibiotic such as amoxicillin, to a method for preparing said tablet and to the use of said tablet.

Claims (24)

1. A noncoated dispersible tablet comprising a β-lactam antibiotic, from 0.65-1.6% by weight of the tablet of a disintegrant, characterized in that said disintegrant comprises crospovidone which is present in an amount of 0.80±0.15% by weight of the tablet, and one or more pharmaceutically acceptable excipients, wherein the β-lactam antibiotic, the disintegrant and the pharmaceutically acceptable excipients in the tablet are in the form of a mixture.

2. The tablet according to claim 1 , wherein the β-lactam antibiotic is amoxicillin trihydrate.

3. The tablet according to claim 2 , wherein the amoxicillin trihydrate is present in an amount of from 50% to 97% by weight of the tablet.

4. The tablet according to claim 1 , wherein the tablet comprises less than 500 ppm of a compound selected from the group consisting of dichloromethane, isopropanol, pivalic acid and triethyl amine.

5. The tablet according to claim 1 , wherein the tablet further comprises an additive.

6. The tablet according to claim 5 , wherein the additive comprises at least one of a β-lactamase inhibitor and an artificial flavor.

7. The tablet according to claim 6 , wherein the β-lactamase inhibitor is clavulanic acid or a pharmaceutically acceptable salt thereof.

8. The tablet according to claim 1 , wherein the tablet disintegrates within from 30 to 120 seconds after being placed in water in accordance with section 5.3 of Document QAS/09.324/Final dated March 2011 of the WHO Revision of Monograph on Tablets using water at a temperature of 15-25° C.

9. (Rejoined and Previously Amended) A method for the preparation of a dispersible tablet according to claim 1 comprising the steps of:

(a) sifting tablet components comprising the β-lactam antibiotic, the disintegrant in an amount from 0.65-1.6% by weight of the tablet, the disintegrant comprising crospovidone which is present in an amount of 0.80±0.15% by weight of the tablet, and an optional first group of additives;

(b) mixing the components obtained in step (a) to obtain a mixture thereof;

(c) adding a lubricant to the mixture obtained in step (b); and

(d) compressing the mixture obtained in step (c) into a tablet, wherein the amount of crospovidone is from 0.1-1.6% by weight of said tablet.

10. The method according to claim 9 , wherein the β-lactam antibiotic is amoxicillin trihydrate.

11. The method according to claim 9 , wherein said lubricant is magnesium stearate.

12. A package comprising the tablet according to claim 1 .

13. A noncoated dispersible tablet comprising a β-lactam antibiotic and from 0.65-1.6% by weight of the tablet of a disintegrant which comprises crospovidone, the crospovidone being present in an amount of 0.80±0.15% by weight of the tablet, microcrystalline cellulose, a lubricant and one or more of a flavor and sweetener, wherein the β-lactam antibiotic, disintegrant, microcrystalline cellulose, lubricant and flavor and/or sweetener are in the form of a mixture, and wherein the tablet disintegrates within from 30 to 120 seconds after being placed in water in according with section 5.3 of Document AAS/09.324/Final dated March 2011 of the WHO Revision of Monograph on Tablets using water at a temperature of 15-25° C.

14. The tablet according to claim 13 , wherein the β-lactam antibiotic is amoxicillin trihydrate.

15. The tablet according to claim 14 , wherein the amoxicillin trihydrate is present in an amount of from 50% to 97% by weight of the tablet.

16. The tablet according to claim 13 , wherein the tablet comprises less than 500 ppm of a compound selected from the group consisting of dichloromethane, isopropanol, pivalic acid and triethyl amine.

17. The tablet according to claim 13 , wherein the tablet further comprises an additive.

18. The tablet according to claim 17 , wherein the additive comprises at least one of a β-lactamase inhibitor and an artificial flavor.

19. The tablet according to claim 18 , wherein the β-lactamase inhibitor is clavulanic acid or a pharmaceutically acceptable salt thereof.

20. A package which comprises the tablet according to claim 13 .

Assignments (2)
CHANGE OF NAME Recorded Apr 2, 2019
From: DSM SINOCHEM PHARMACEUTICALS NETHERLANDS B.V.
To: CENTRIENT PHARMACEUTICALS NETHERLANDS B.V.
Reel/Frame 048775/0029 →
ASSIGNMENT OF ASSIGNOR'S INTEREST Recorded Mar 4, 2016
From: LARDÉE, ABRAHAM CORNELIS
To: DSM SINOCHEM PHARMACEUTICALS NETHERLANDS B.V.
Reel/Frame 037890/0048 →
Priority Claims (1)
EP 13185368 · Sep 20, 2013 · regional
Continuity (1)
Related Publication 20160193153A1 · Jul 7, 2016