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Challenges faced during Albendazole impurity analysis include the sensitivity of analytical methods and the potential variability of impurity levels between batches.
Process-related impurities in Albendazole arise during manufacturing, while degradation impurities occur during the storage or handling of the drug product.
Impurities in Albendazole are controlled during manufacturing with process optimization, careful selection of raw materials, and appropriate analytical testing throughout the production process.
Albendazole impurities are stored at a controlled room temperature between 2-8 °C or as indicated on the Certificate of Analysis (CoA).
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