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Higher levels of impurities in Levothyroxine may impact its therapeutic response, efficacy, or consistency, necessitating strict control measures during manufacturing.
Some Levothyroxine impurities may undergo chemical transformations or degradation during storage, which can affect the overall purity and stability of the drug.
Some impurities may interfere with the pharmacokinetics or pharmacodynamics of Levothyroxine, potentially impacting its interactions with other medicines.
Levothyroxine impurities should be stored at a controlled room temperature, usually between 2-8 °C.
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