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

Label

OXYTOCIN 
oxytocin injection, solution
Product Information
Product TypeHUMAN PRESCRIPTION DRUG LABELItem Code (Source)NDC:52533-050
Route of AdministrationINTRAVENOUSDEA Schedule    
Active Ingredient/Active Moiety
Ingredient NameBasis of StrengthStrength
OXYTOCIN (OXYTOCIN) OXYTOCIN2 [USP'U]  in 100 mL
Inactive Ingredients
Ingredient NameStrength
Sodium Chloride9 g  in 100 mL
Water 
Other Ingredients
Ingredient KindIngredient NameQuantity
May containACETIC ACID 
May containSODIUM HYDROXIDE 
Packaging
#Item CodePackage DescriptionMarketing Start DateMarketing End Date
1NDC:52533-050-30500 mL in 1 BAG
Marketing Information
Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
unapproved drug other11/09/2012
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