01455nam 2200373Ia 450 991069709270332120230902161905.0(CKB)5470000002383971(OCoLC)587646051(EXLCZ)99547000000238397120100330d1997 ua 0enguran|||||||||txtrdacontentcrdamediacrrdacarrierGuidance for industry[electronic resource] nonsterile semisolid dosage forms : scale-up and postapproval changes : chemistry, manufacturing, and controls : in vitro release testing and in vivo bioequivalence documentationRockville, MD :U.S. Dept. of Health and Human Services, Food and Drug Administration, Center for Drug Evaluation and Research,[1997]1 electronic resource (30) pages'SUPAC-SS.""CMC 7."Includes bibliographical references (29).Guidance for industry DrugsDosage formsUnited StatesTestingDrugsTherapeutic equivalencyDocumentationUnited StatesDrugsDosage formsTesting.DrugsTherapeutic equivalencyDocumentationCenter for Drug Evaluation and Research (U.S.)GPOGPOBOOK9910697092703321Guidance for industry3434577UNINA