参考原辅料相容性试验结果，通过溶出度及稳定性等实验进行辅料种类及用量的

With reference to the results of the compatibility test of raw materials and excipients, the types and dosages of auxiliary materials are screened through experiments such as dissolution and stability, and the types and dosages of the used auxiliary materials are determined to be within the oral administration route and dosage range prescribed by the FDA Inactive Ingredient Database (IIG) Within, and all are pharmaceutical grade excipients with legal origin.

Reference to the results of the original auxiliary compatibility test, through the solubility and stability of the experiment to screen the type and dosage of the auxiliary material, to determine that the type and dosage of the auxiliary materialused are in the FDA inactive ingredientdatabase database (IIG) prescribed oral administration path and dosage range, and are within the legal source of pharmaceutical grade auxiliary materials.

According to the results of compatibility test of raw and auxiliary materials, the types and dosage of auxiliary materials were screened through dissolution and stability experiments, and it was determined that the types and dosage of auxiliary materials were within the oral administration route and dosage range specified by the FDA inactive ingredient database (iig), and they were all pharmaceutical grade auxiliary materials with legal sources.<br>