Is the imprint requirement for solid oral dosage units applicable only to tablets?

The imprint requirement for solid oral dosage units applies to both tablets and capsules, making the assertion that it is only applicable to tablets inaccurate. The purpose of the imprint is to provide a unique identification for the dosage form, which aids in preventing medication errors and ensuring patient safety.

This requirement helps healthcare professionals and patients distinguish between different medications, including various strengths, formulations, and manufacturers. Both tablets and capsules can come in various shapes and colors, and without an imprint, it would be much more challenging to verify the identity of the medication. In turn, this would increase the risk of medication errors and potentially endanger patient health.

Therefore, the requirement is not limited to just tablets or any specific category of medication, which confirms that the correct response is that the imprint requirement applies broadly, making the answer true to the wider context of solid oral dosage units.