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  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 OXYTOCIN (OXYTOCIN) OXYTOCIN 2 [USP'U]  in 100 mL

Inactive Ingredients Ingredient Name Strength WATER   SODIUM CHLORIDE 600 mg  in 100 mL SODIUM LACTATE 310 mg  in 100 mL POTASSIUM CHLORIDE 30 mg  in 100 mL CALCIUM CHLORIDE 20 mg  in 100 mL DEXTROSE MONOHYDRATE 5 g  in 100 mL

Product Characteristics Color      Score      Shape Size Flavor Imprint Code Contains

Packaging # Item Code Package Description Multilevel Packaging 1 NDC:52533-050-44 1000 mL in 1 BAG None

Marketing Information
Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
unapproved drug other		10/18/2012	12/04/2012

Labeler - Cantrell Drug Company (035545763)

Revised: 11/2012 Cantrell Drug Company