Ivosidenib - Isotope Labelled Standards
References
FAQ's
References
Frequently Asked Questions
How are Ivosidenib impurities reported in the drug's labeling information?
Impurities in Ivosidenib are in the drug's labeling information, including the package insert or prescribing information. This information may provide details on the impurity profile, acceptable limits, and potential risks with impurities.
Can Ivosidenib impurities be removed or reduced during the manufacturing process?
Manufacturers use purification techniques and optimized manufacturing processes to minimize impurities in Ivosidenib. These measures aim to remove or reduce them to ensure the highest possible purity of the final product.
Which solvent helps in analyzing Ivosidenib impurities?
Methanol is commonly used as a solvent when analyzing the impurities in Ivosidenib.
How should Ivosidenib impurities be stored in terms of temperature?
The recommendation is to store Ivosidenib impurities at a controlled room temperature, within 2-8 °C.
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