1、Conclusion Famotidine is passively absorbed by transferring the intestine.
結(jié)論法莫替丁在腸道的吸收為被動擴(kuò)散。

2、Famotidine dispersible tablets were prepared by direct compression method.
采用全粉末直接壓片法制備法莫替丁分散片。

3、The conclusion is famotidine could excite antral myoelectric activity.
提示法莫替丁可興奮胃竇肌電活動。

4、AIM: To study the effect of famotidine on the pharmacokinetics of domperidone.
目的：觀察法莫替丁對多潘立酮藥代動力學(xué)的影響。

5、The study examine the drug release mechanism of famotidine chitosan microcapsule.
初步研究了法莫替丁-甲殼胺微囊的釋藥機(jī)理。

6、OBJECTIVE:To compare the bioequivalence between famotidine chewing tablets and commercial tablets.
目的：比較法莫替丁咀嚼片、普通片的人體生物等效性。

7、OBJECTIVE: To prepare sustained-release famotidine tablet and evaluate its drug release property.
目的：制備法莫替丁緩釋片劑，并評價其釋放特性。

8、Objective:A HPLC method was developed to determine the related substances of Famotidine Injection.
目的：檢查法莫替丁注射液中的有關(guān)物質(zhì)。