The body absorption rate of the active ingredient affects the drug efficacy. Therefore, disintegration test and dissolution test are important for orally ingested tablets. These tests shall be carried out under prescribed conditions according to specific applicable Pharmacopoeial standards. All of our standard solutions and reagents for disintegration and dissolution test comply with the Japanese Pharmacopoeia.
- Adopted a container of low elution type
- Issuing QC report with information on raw materials used
- Display expiration date on label
- Employing clean bottle for highly pure chemical with tamper-proof lid
Produced under well-controlled clean condition
Appearance for container (5L & 10L)
- Open All
- Close All
Higher Concentrated solution
Calibration standard (by USP)
For research use or further manufacturing use only. Not for use in diagnostic procedures.
Product content may differ from the actual image due to minor specification changes etc.
If the revision of product standards and packaging standards has been made, there is a case where the actual product specifications and images are different.