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The effect of impurities on the shelf life of Cefdinir depends on the specific impurity class and the storage conditions of the drug. Impurities reduce the drug's potency and efficacy by degradation. Further, their presence in the drug product may also accelerate the breakdown of the drug, leading to a shorter shelf life.
Analytical techniques such as HPLC and LC-MS help monitor Cefdinir impurities during manufacturing.
DMSO is a solvent to analyze Cefdinir and its impurities.
Cefdinir impurities should be stored at a controlled room temperature between 2-8 ⁰C or as indicated on the Certificate of Analysis (CoA).
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