摘要
本文按美国药典21版第4补充本收载的螺内酯片溶出度测定的具体规定,对国产五厂七批螺内酯片及胶囊进行溶出度考察,结果其中6个批号均符合规定,仅一个批号因工艺不合理而不符合规定.
Acoording to the method for the test of spironolactone tablets dissolution ratespecified in USPⅩⅪ 4th supplement,7 Batches of the tablets and capsules from5 factories in china were determined.It was found that 6 of them complied withthe requirement one failed due to the unperfect technology of the production.
出处
《中国医院药学杂志》
CAS
CSCD
北大核心
1990年第6期246-248,共3页
Chinese Journal of Hospital Pharmacy
关键词
螺内酯
片剂
胶囊剂
溶出度
Tab
Spironolactone
Capsules
Dissolution Rate
