Your browser does not support JavaScript! FENTANYL CITRATE INJECTION, SOLUTION [CANTRELL DRUG COMPANY]
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RxNorm Names

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.
Drug Label Sections

Label

FENTANYL CITRATE 
fentanyl citrate injection, solution
Product Information
Product TypeHUMAN PRESCRIPTION DRUG LABELItem Code (Source)NDC:52533-025
Route of AdministrationINTRAVENOUSDEA ScheduleCII    
Active Ingredient/Active Moiety
Ingredient NameBasis of StrengthStrength
Fentanyl Citrate (Fentanyl) Fentanyl20 ug  in 1 mL
Inactive Ingredients
Ingredient NameStrength
Sodium Chloride9 mg  in 1 mL
Water 
Packaging
#Item CodePackage Description
1NDC:52533-025-75100 mL in 1 BAG
Marketing Information
Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
unapproved drug other01/30/2013
Labeler - Cantrell Drug Company (035545763)

Revised: 05/2013
Document Id: 0a6669a6-692d-4dd6-b9de-66b60e215983
Set id: f98ebc12-05ac-4777-9eb5-642fb8124b50
Version: 3
Effective Time: 20130515
 
Cantrell Drug Company

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