It is a specified impurity that forms when Amlodipine interacts with glucose and galactose, commonly occurring during storage.

It is monitored to ensure quality and safety in Amlodipine formulations, adhering to regulatory guidelines.

It forms as a reaction product between Amlodipine and sugars like glucose and galactose, typically under certain storage conditions.

Formation can be managed by controlling storage conditions and implementing regular testing.

Detection and quantification of Amlodipine Glucose and Galactose Adduct utilize advanced methods like GC-MS, LC-MS, and HPLC-MS.

Chemicea provides COA, H-NMR, MASS, HPLC, and TGA reports as standard, with additional documents available upon request.

Yes, Chemicea\'s documentation meets standards required by major regulatory bodies like the FDA, EMA, and other authorities.

Amlodipine Glucose and Galactose Adduct is stable for shipping at room temperature, with specific storage guidelines provided in the COA.

Yes, both standard and customized pack sizes are available based on client requirements.

Chemicea provides Amlodipine Glucose and Galactose Adduct as a reference standard, supporting impurity analysis, validation, and regulatory compliance.