Ezetimibe tablet 10 mg product-specific bioequivalence guidance

Draft

We have adopted this International Scientific Guideline - EMA/CHMP/802491/2018.

Last updated

3 June 2024

About this guideline

End of consultation (overseas): 30 June 2019

Categories: Clinical pharmacology and pharmacokinetics | Product-specific bioequivalence

TGA annotations: Nil

Where EU guidelines adopted in Australia include references to EU legislation (including EC Directives and Regulations), the requirements contained in the referenced EU legislation are not applicable to the evaluation of medicines by the TGA.
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