介紹了“901”復(fù)方感冒沖劑的工藝、質(zhì)量控制及穩(wěn)定性。制得的沖劑符合中國藥典（1990版）的要求；對其主藥黃芩、柴胡進行了薄層定性鑒別；以黃芩甙為指標，采用一階導(dǎo)數(shù)光譜法進行了含量測定；加速實驗預(yù)測有效期為1.97年。

The manufacturing process, quality Control and Stability test of ＂901＂ anti-influenza complex granule were presented. The granule tallied with requirements of Chinese Pharmacopiea (1990th edition). It s main components (Scutellaria baicallensis Georgi. and Bupleurum chinese DC.) were identified with TLC. First derivative spectrometry was used to determine the content of baicalin in this preparation. As a result of stability test, the shelf life at 250℃ is estimated to be 1.97 years.