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


Category DEA Schedule Marketing Status
HUMAN PRESCRIPTION DRUG LABEL CII 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.
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Label

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FENTANYL CITRATE 
fentanyl citrate injection, solution
Product Information
Product TypeHUMAN PRESCRIPTION DRUG LABELItem Code (Source)NDC:52533-024
Route of AdministrationINTRAVENOUSDEA ScheduleCII    
Active Ingredient/Active Moiety
Ingredient NameBasis of StrengthStrength
FENTANYL CITRATE (FENTANYL) FENTANYL CITRATE10 ug  in 1 mL
Inactive Ingredients
Ingredient NameStrength
SODIUM CHLORIDE9 mg  in 1 mL
WATER 
Packaging
#Item CodePackage Description
1NDC:52533-024-01100 mL in 1 BAG
Marketing Information
Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
unapproved drug other04/13/2012
Labeler - Cantrell Drug Company (035545763)
Establishment
NameAddressID/FEIBusiness Operations
Cantrell Drug Company035545763manufacture(52533-024)

Revised: 10/2012
Document Id: dec8a56e-c2b5-4917-8c26-8594fb3c02f2
Set id: a2603cb4-a700-420e-aee5-58f6838567ab
Version: 1
Effective Time: 20121009
 
Cantrell Drug Company

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