What does a successful New Drug Application (NDA) result in?

A successful New Drug Application (NDA) results in market approval for a new drug by the FDA, which is critical for ensuring that new medications can be sold and marketed to healthcare providers and patients. The NDA process involves a thorough review of data regarding the drug's safety and efficacy, including clinical trial results. This evaluation is essential to ensure that the new drug meets the necessary regulatory standards before it can be considered for use in the general population.

Market approval from the FDA confirms that the drug has gone through the rigorous testing and evaluation required to demonstrate its benefits outweigh potential risks, hence providing assurance to both healthcare professionals and consumers about the drug's quality and effectiveness. The NDA does not eliminate regulations surrounding drug manufacturing; instead, it ensures compliance with these regulations prior to approval for public use.