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 20 USP Units Added to Lactated Ringer's 1,000 mL Bag

Label

OXYTOCIN 
oxytocin injection, solution
Product Information
Product Type HUMAN PRESCRIPTION DRUG Item Code (Source) NDC:52533-051
Route of Administration INTRAVENOUS DEA Schedule     
Active Ingredient/Active Moiety
Ingredient Name Basis of Strength Strength
OXYTOCIN (UNII: 1JQS135EYN) (OXYTOCIN - UNII:1JQS135EYN) OXYTOCIN 2 [USP'U]  in 100 mL
Inactive Ingredients
Ingredient Name Strength
WATER (UNII: 059QF0KO0R)  
SODIUM CHLORIDE (UNII: 451W47IQ8X) 600 mg  in 100 mL
SODIUM LACTATE (UNII: TU7HW0W0QT) 310 mg  in 100 mL
POTASSIUM CHLORIDE (UNII: 660YQ98I10) 30 mg  in 100 mL
CALCIUM CHLORIDE (UNII: M4I0D6VV5M) 20 mg  in 100 mL
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:52533-051-24 1000 mL in 1 BAG
Marketing Information
Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date
unapproved drug other 10/20/2011
Labeler - Cantrell Drug Company (035545763)

Revised: 1/2015
Document Id: ecd8aa21-89cf-47e7-bb2f-5f1457e46602
Set id: 447c07c9-5343-4370-b046-5725a7e45398
Version: 5
Effective Time: 20150116
 
Cantrell Drug Company