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Extended-release ER refers to a type of medication that is formulated to release the active ingredient slowly over an extended period of time.
Manufacturers of medications that are classified as extended-release ER are required to file the necessary documentation with regulatory authorities.
To fill out extended-release ER documentation, manufacturers must provide detailed information about the medication's formulation, release mechanism, and intended use.
The purpose of extended-release ER medications is to provide a prolonged and controlled release of the active ingredient, leading to sustained therapeutic effects.
Information that must be reported on extended-release ER documentation includes details about the drug's formulation, release profile, bioavailability, and safety profile.
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