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Lilly AMP is the Abbreviated New Drug Application (ANDA) submission and approval process for generic drugs.
Generic drug manufacturers are required to file an application for Lilly AMP.
The application for Lilly AMP must be filled out following the guidelines provided by the FDA.
The purpose of the Lilly AMP application is to gain approval for the marketing and sale of generic drugs.
The Lilly AMP application must include detailed information on the generic drug formulation, manufacturing process, labeling, and bioequivalence studies.
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