01383nam 2200385Ia 450 991069937800332120230902162200.0(CKB)5470000002402133(OCoLC)499109706(EXLCZ)99547000000240213320100115d2006 ua 0enguran|||||||||txtrdacontentcrdamediacrrdacarrierGuidance for industry[electronic resource] labeling for human prescription drug and biological products, implementing the new content and format requirementsRockville, MD :U.S. Dept. of Health and Human Services, Food and Drug Administration, Center for Drug Evaluation and Research :Center for Biologics Evaluation and Research,[2006]1 online resource (27 pages)"Draft guidance.""Labeling.""January 2006."Guidance for industry DrugsLabelingBiologicalsLabelingDrugsLabeling.BiologicalsLabeling.Center for Drug Evaluation and Research (U.S.)Center for Biologics Evaluation and Research (U.S.)GPOGPOBOOK9910699378003321Guidance for industry3434577UNINA