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 30 USP Units Added to Lactated Ringer's 500 mL Bag

Label

OXYTOCIN 
oxytocin injection, solution
Product Information
Product Type HUMAN PRESCRIPTION DRUG Item Code (Source) NDC:52533-055
Route of Administration INTRAVENOUS DEA Schedule     
Active Ingredient/Active Moiety
Ingredient Name Basis of Strength Strength
OXYTOCIN (UNII: 1JQS135EYN) (OXYTOCIN - UNII:1JQS135EYN) OXYTOCIN 30 [USP'U]  in 500 mL
Inactive Ingredients
Ingredient Name Strength
SODIUM CHLORIDE (UNII: 451W47IQ8X) 3 g  in 500 mL
SODIUM LACTATE (UNII: TU7HW0W0QT) 1.55 g  in 500 mL
POTASSIUM CHLORIDE (UNII: 660YQ98I10) 0.15 g  in 500 mL
CALCIUM CHLORIDE (UNII: M4I0D6VV5M) 0.1 g  in 500 mL
WATER (UNII: 059QF0KO0R)  
Other Ingredients
Ingredient Kind Ingredient Name Quantity
May contain ACETIC ACID (UNII: Q40Q9N063P)  
May contain HYDROCHLORIC ACID (UNII: QTT17582CB)  
Packaging
# Item Code Package Description Marketing Start Date Marketing End Date
1 NDC:52533-055-30 500 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: 12/2014
Document Id: 3b5b2071-da23-4d84-bdbe-02cf7a4afc6b
Set id: 736b2590-79e8-4bd0-ab54-84ff7e29a030
Version: 5
Effective Time: 20141224
 
Cantrell Drug Company