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To facilitate the development of an ANDA, agency provides the following resources on ANDA forms and submission requirements.
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An Abbreviated New Drug Application (ANDA) is a submission to the FDA for the approval of generic drugs, demonstrating that the proposed drug is equivalent in safety, efficacy, and quality to
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Learn more An abbreviated new drug application (ANDA) contains data which is submitted to FDA for the review and potential approval of a generic drug product.
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