Solid pharmaceutical preparation containing levothyroxine

1. A solid pharmaceutical preparation comprising levothyroxine sodium, 2-10% by weight based on the preparation of gelatine, 0.2 to 3% by weight based on the preparation of citric acid, and a filler that is 50 to 80% by weight, based on the preparation, of mannitol, sucrose or lactose, and 10 to 30% by weight, based on the preparation, of maize starch.

2. The solid pharmaceutical preparation according to claim 1 , further comprising liothyronine sodium.

3. The solid pharmaceutical preparation according to claim 1 , wherein the filler is sucrose.

4. The solid pharmaceutical preparation according to claim 1 , wherein filler is mannitol and maize starch.

5. The solid pharmaceutical preparation according to claim 1 , further comprising an antioxidant that is tocopherol, propyl gallate, tertiary butylhydroquinone, butylated hydroxyanisole or butylated hydroxytoluene.

6. The solid pharmaceutical preparation according to claim 5 , wherein the antioxidant is butylated hydroxyanisole or butylated hydroxytoluene.

7. The solid pharmaceutical preparation according to claim 1 , in granule, pellet, capsule or tablet form.

8. The solid pharmaceutical preparation according to claim 7 , that is a tablet.

9. The solid pharmaceutical preparation according to claim 1 , wherein at least one disintegrating agent is present.

10. The solid pharmaceutical preparation according to claim 9 , wherein the disintegrating agent is sodium starch glycolate, carboxymethylcellulose sodium or a mixture thereof.

11. The solid pharmaceutical preparation according to claim 10 , wherein the disintegrating agent present is carboxymethylcellulose sodium.

12. The solid pharmaceutical preparation according to claim 1 , comprising 0.05 to 0.5% by weight butylated hydroxytoluene.

13. The solid pharmaceutical preparation according to claim 1 , comprising 0.4-2% citric acid.

14. A process for the production of a solid pharmaceutical preparation according to claim 8 , comprising suspending

(a) levothyroxine sodium and optionally liothyronine sodium in an aqueous gelatine solution,

(b) spraying the suspension obtained in (a) onto the filler in a fluidized bed granulation and drying to form granules, citric acid being either dissolved in the aqueous gelatine solution or admixed with the granules,

(c) collecting the granules obtained in (b) and optionally,

(d) mixing a disintegrant and optionally a lubricant with the granules obtained in (c), and

(e) compressing a mixture obtained in (d) to give tablets.

15. The process for the production of a solid pharmaceutical preparation according to claim 14 , wherein an antioxidant is dissolved in the aqueous gelatine solution used in (a) or is admixed with the granules in (d).

16. The process for the preparation of a solid pharmaceutical preparation according to claim 14 , wherein the granules or the tablets are provided with a coating.

17. A process for the stabilization of levothyroxine sodium, comprising adding to a composition of said levothyroxine sodium a stabilizing-effective amount of gelatine, citric acid and a filler that is sucrose, mannitol or lactose and maize starch, whereby said composition contains, by weight, based on the composition, 2-10% gelatine, 0.2-3% citric acid, 50-80% mannitol, sucrose or lactose and 10 to 30% maize starch.

18. The process according to claim 17 , wherein the filler is mannitol and maize starch.