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 10 USP Units Added to 0.9% Sodium Chloride 500 mL Bag


oxytocin injection, solution
Product Information
Product Type HUMAN PRESCRIPTION DRUG Item Code (Source) NDC:52533-050
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) 9 g  in 100 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:52533-050-30 500 mL in 1 BAG
Marketing Information
Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date
unapproved drug other 11/09/2012
Labeler - Cantrell Drug Company (035545763)

Revised: 12/2014
Document Id: 886dc21d-dbb7-4f61-82c6-dc2baf59bb61
Set id: aae73dac-d092-4163-8a37-f1a7459a4217
Version: 5
Effective Time: 20141211
Cantrell Drug Company