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In accordance with the guidelines outlined in the National Medical Products Administration (NMPA) Technical Guideline for Bioequivalence Studies of Generic Chemical Drugs with Pharmacokinetic Parameters as the Endpoints, and considering the characteristics of the drug used in this study, the overall design was a single-center, open-label, randomized, two-formulation, two-period, two-way crossover, fasting pharmacokinetic study

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No signs of lipid accumulation, inflammation, or necrosis were observed

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