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 1 mL Syringe

Label

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 10 ug  in 1 mL
Inactive Ingredients
Ingredient Name Strength
Sodium Chloride (UNII: 451W47IQ8X) 9 mg  in 1 mL
Water (UNII: 059QF0KO0R)  
Other Ingredients
Ingredient Kind Ingredient Name Quantity
May contain HYDROCHLORIC ACID (UNII: QTT17582CB)  
May contain SODIUM HYDROXIDE (UNII: 55X04QC32I)  
Packaging
# Item Code Package Description Marketing Start Date Marketing End Date
1 NDC:52533-024-45 1 mL in 1 SYRINGE, PLASTIC 01/30/2013
Marketing Information
Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date
unapproved drug other 01/30/2013
Labeler - Cantrell Drug Company (035545763)

Revised: 5/2014
Document Id: a6d6c5df-48a8-4d78-a5b1-4222122b6e8b
Set id: 62752ca3-060e-430b-a05c-40c89ee5df1d
Version: 5
Effective Time: 20140502
 
Cantrell Drug Company