Your browser does not support JavaScript! CEFAZOLIN SODIUM INJECTION, SOLUTION [CANTRELL DRUG COMPANY]
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CEFAZOLIN SODIUM injection, solution
[Cantrell Drug Company]


Category DEA Schedule Marketing Status
HUMAN PRESCRIPTION DRUG LABEL unapproved drug other
NOTE:THIS DRUG HAS NOT BEEN FOUND BY FDA TO BE SAFE AND EFFECTIVE, AND THIS LABELING HAS NOT BEEN APPROVED BY FDA. For further information about unapproved drugs, click here.
Drug Label Sections

Label

Label

CEFAZOLIN SODIUM 
cefazolin sodium injection, solution
Product Information
Product TypeHUMAN PRESCRIPTION DRUG LABELItem Code (Source)NDC:52533-015
Route of AdministrationINTRAVENOUSDEA Schedule    
Active Ingredient/Active Moiety
Ingredient NameBasis of StrengthStrength
Cefazolin Sodium (Cefazolin) Cefazolin Sodium2 g  in 100 mL
Inactive Ingredients
Ingredient NameStrength
Dextrose5 g  in 100 mL
Water 
Packaging
#Item CodePackage Description
1NDC:52533-015-14100 mL in 1 BAG
Marketing Information
Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
unapproved drug other09/30/2011
Labeler - Cantrell Drug Company (035545763)

Revised: 11/2012
Document Id: 7cbbdb5e-fafc-4547-9cfa-705755820f4f
Set id: b3cbf77e-24fb-4237-8d2e-2fe47ce3abef
Version: 3
Effective Time: 20121113
 
Cantrell Drug Company

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