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 1,000 mL Bag

Preparation Label

OXYTOCIN 
oxytocin injection, solution
Product Information
Product TypeHUMAN PRESCRIPTION DRUGItem Code (Source)NDC:52533-048
Route of AdministrationINTRAVENOUS
Active Ingredient/Active Moiety
Ingredient NameBasis of StrengthStrength
OXYTOCIN (UNII: 1JQS135EYN) (OXYTOCIN - UNII:1JQS135EYN) OXYTOCIN10 [USP'U]  in 1000 mL
Inactive Ingredients
Ingredient NameStrength
SODIUM CHLORIDE (UNII: 451W47IQ8X) 9 g  in 1000 mL
WATER (UNII: 059QF0KO0R)  
Other Ingredients
Ingredient KindIngredient NameQuantity
May containACETIC ACID (UNII: Q40Q9N063P)  
May containSODIUM HYDROXIDE (UNII: 55X04QC32I)  
Packaging
#Item CodePackage DescriptionMarketing Start DateMarketing End Date
1NDC:52533-048-241000 mL in 1 BAG
Marketing Information
Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
unapproved drug other07/30/2012
Labeler - Cantrell Drug Company (035545763)

Revised: 12/2014
Document Id: b9f98eaf-6261-49f5-81dc-e1c212bdb34f
Set id: dbba90dd-e29c-41fc-b2e9-8c1af162586b
Version: 8
Effective Time: 20141211
 
Cantrell Drug Company