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035   $a(CKB)5470000002402051
035   $a(OCoLC)497212892
035   $a(EXLCZ)995470000002402051
100   $a20100112d2007      ua             0
101 0 $aeng
135   $auran|||||||||
181   $ctxt$2rdacontent
182   $cc$2rdamedia
183   $acr$2rdacarrier
200 00$aGuidance for industry$b[electronic resource] $edosage and administration section of labeling for human prescription drug and biological products, content and format
210  1$aRockville, MD :$cU.S. Dept. of Health and Human Services, Food and Drug Administration, Center for Drug Evaluation and Research :$cCenter for Biologics Evaluation and Research,$d[2007]
215   $a1 online resource (i, 10 pages)
300   $a"Draft guidance."
300   $a"Labeling."
300   $a"April 2007."
517   $aGuidance for industry 
606   $aDrugs$xLabeling
606   $aDrugs$xDosage
606   $aBiologicals$xLabeling
615  0$aDrugs$xLabeling.
615  0$aDrugs$xDosage.
615  0$aBiologicals$xLabeling.
712 02$aCenter for Drug Evaluation and Research (U.S.)
712 02$aCenter for Biologics Evaluation and Research (U.S.)
801  0$bGPO
801  1$bGPO
906   $aBOOK
912   $a9910699386203321
996   $aGuidance for industry$93434577
997   $aUNINA