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() Delayed Release Tablets DESCRIPTION Each delayed release tablet for oral administration contains 1.2g 5aminosalicylic acid (5ASA;), an antiinflammatory agent. Also has the chemical name 5amino2hydroxybenzoic

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What is delayed release tablets description?

Delayed release tablets description refers to a detailed explanation of how a specific medication in tablet form is designed to be released in the body over a certain period of time.

Who is required to file delayed release tablets description?

Pharmaceutical companies or manufacturers are typically required to file delayed release tablets description with regulatory authorities.

How to fill out delayed release tablets description?

Delayed release tablets description can be filled out by providing information on the composition of the tablet, the release mechanism used, and any specific instructions for taking the medication.

What is the purpose of delayed release tablets description?

The purpose of delayed release tablets description is to ensure that healthcare professionals and patients understand how the medication works and how it should be taken for optimal effectiveness.

What information must be reported on delayed release tablets description?

Information that must be reported on delayed release tablets description includes the active ingredients, dosage strength, release profile, potential side effects, and any special storage instructions.

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