附录1压缩剂型溶出度试验要求

{"title":"附录1压缩剂型溶出度试验要求","authors":"Sarfaraz K Niazi","doi":"10.1201/b14437-6","DOIUrl":null,"url":null,"abstract":"","PeriodicalId":238873,"journal":{"name":"Handbook of Pharmaceutical Manufacturing Formulations, Second Edition","volume":"67 1","pages":"0"},"PeriodicalIF":0.0000,"publicationDate":"2019-07-17","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":"0","resultStr":"{\"title\":\"Appendix I Dissolution Testing Requirements of Compressed Dosage Forms\",\"authors\":\"Sarfaraz K Niazi\",\"doi\":\"10.1201/b14437-6\",\"DOIUrl\":null,\"url\":null,\"abstract\":\"\",\"PeriodicalId\":238873,\"journal\":{\"name\":\"Handbook of Pharmaceutical Manufacturing Formulations, Second Edition\",\"volume\":\"67 1\",\"pages\":\"0\"},\"PeriodicalIF\":0.0000,\"publicationDate\":\"2019-07-17\",\"publicationTypes\":\"Journal Article\",\"fieldsOfStudy\":null,\"isOpenAccess\":false,\"openAccessPdf\":\"\",\"citationCount\":\"0\",\"resultStr\":null,\"platform\":\"Semanticscholar\",\"paperid\":null,\"PeriodicalName\":\"Handbook of Pharmaceutical Manufacturing Formulations, Second Edition\",\"FirstCategoryId\":\"1085\",\"ListUrlMain\":\"https://doi.org/10.1201/b14437-6\",\"RegionNum\":0,\"RegionCategory\":null,\"ArticlePicture\":[],\"TitleCN\":null,\"AbstractTextCN\":null,\"PMCID\":null,\"EPubDate\":\"\",\"PubModel\":\"\",\"JCR\":\"\",\"JCRName\":\"\",\"Score\":null,\"Total\":0}","platform":"Semanticscholar","paperid":null,"PeriodicalName":"Handbook of Pharmaceutical Manufacturing Formulations, Second Edition","FirstCategoryId":"1085","ListUrlMain":"https://doi.org/10.1201/b14437-6","RegionNum":0,"RegionCategory":null,"ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"","PubModel":"","JCR":"","JCRName":"","Score":null,"Total":0}