OXYTOCIN - oxytocin 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.


Oxytocin 15 USP Units Added to 0.9% Sodium Chloride 250 mL Bag

image description

oxytocin injection, solution
Product Information
Product Type HUMAN PRESCRIPTION DRUG Item Code (Source) NDC:52533-056
Route of Administration INTRAVENOUS DEA Schedule     
Active Ingredient/Active Moiety
Ingredient Name Basis of Strength Strength
Inactive Ingredients
Ingredient Name Strength
Sodium Chloride (UNII: 451W47IQ8X) 2.25 g  in 250 mL
Water (UNII: 059QF0KO0R)  
Other Ingredients
Ingredient Kind Ingredient Name Quantity
May contain ACETIC ACID (UNII: Q40Q9N063P)  
May contain SODIUM HYDROXIDE (UNII: 55X04QC32I)  
# Item Code Package Description Marketing Start Date Marketing End Date
1 NDC:52533-056-18 250 mL in 1 BAG
Marketing Information
Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date
unapproved drug other 04/25/2013
Labeler - Cantrell Drug Company (035545763)

Revised: 12/2014
Document Id: 33dae4b1-7018-459f-a8fe-a6b0059e9445
Set id: aefa8a81-43ee-40db-8d75-8eff70c65ca6
Version: 2
Effective Time: 20141211
Cantrell Drug Company