Fed Regist. 2006 Aug 1;71(147):83358[sic., should be 43358]-63.
The Food and Drug Administration (FDA) is issuing a final rule to amend the final monograph (FM) for over-the-counter (OTC) nasal decongestant drug products (drug products used to relieve nasal congestion due to a cold, hay fever, or other upper respiratory allergies) to add phenylephrine bitartrate (PEB), both individually and in combination drug products in an effervescent dosage form, as generally recognized as safe and effective (GRASE). An effervescent dosage form is intended to be dissolved in water before taking by mouth. This final rule is part of FDA's ongoing review of OTC drug products.
美国食品药品监督管理局(FDA)正在发布一项最终规则,修订非处方(OTC)鼻用减充血剂药品(用于缓解因感冒、花粉热或其他上呼吸道过敏引起的鼻充血的药品)的最终专论(FM),以将酒石酸去氧肾上腺素(PEB)单独以及以泡腾剂型的复方药品形式添加进去,认定其一般认为安全有效(GRASE)。泡腾剂型旨在口服前溶于水中。本最终规则是FDA对OTC药品持续审查的一部分。