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.

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

image description

OXYTOCIN 
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
OXYTOCIN (UNII: 1JQS135EYN) (OXYTOCIN - UNII:1JQS135EYN) OXYTOCIN 15 [USP'U]  in 250 mL
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)  
Packaging
# 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