FENTANYL CITRATE- fentanyl citrate injection, solution 
Cantrell Drug Company

Disclaimer: 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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Fentanyl Citrate 10 mcg/mL in 0.9% Sodium Chloride 100 mL Bag

Label

image description

FENTANYL CITRATE 
fentanyl citrate injection, solution
Product Information
Product Type HUMAN PRESCRIPTION DRUG Item Code (Source) NDC:52533-024
Route of Administration INTRAVENOUS DEA Schedule CII    
Active Ingredient/Active Moiety
Ingredient Name Basis of Strength Strength
FENTANYL CITRATE (UNII: MUN5LYG46H) (FENTANYL - UNII:UF599785JZ) FENTANYL CITRATE 10 ug  in 1 mL
Inactive Ingredients
Ingredient Name Strength
SODIUM CHLORIDE (UNII: 451W47IQ8X) 9 mg  in 1 mL
WATER (UNII: 059QF0KO0R)  
Packaging
# Item Code Package Description Marketing Start Date Marketing End Date
1 NDC:52533-024-01 100 mL in 1 BAG
Marketing Information
Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date
unapproved drug other 04/13/2012
Labeler - Cantrell Drug Company (035545763)
Establishment
Name Address ID/FEI Business Operations
Cantrell Drug Company 035545763 manufacture(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