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各省、自治区、直辖市及计划单列市卫生厅(局): 根据《中华人民共和国药品管理法》第二十三条的规定,现予颁布《中华人民共和国药典》(简称“中国药典”)一九九○年版一、二两部,自一九九一年七月一日起正式执行。 现就执行中的有关问题通知如下: 一、一九九○年版中国药典正式执行后,原一九八五年版中国药典同品种标准即停止执行,一九九一年七月一日前生产的药品,可按原标准进行检验。
Health Bureau (Bureau) of each province, autonomous region, municipality directly under the Central Government and cities specifically designated in the plan: According to Article 23 of the “Drug Administration Law of the People’s Republic of China”, promulgation of the “Pharmacopoeia of the People’s Republic of China” (hereinafter referred to as “Chinese Pharmacopoeia”) 1990 edition of one or two, since July 1, 1991 formally implemented. The relevant issues concerning the implementation are hereby notified as follows: 1. After the formal implementation of the Chinese Pharmacopoeia of the 1990 edition, the original version of the Chinese Pharmacopoeia for the same version of the 1985 version of the Chinese Pharmacopoeia ceases to be implemented. The drugs manufactured before July 1, 1991 , According to the original standard test.