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 5% Dextrose/0.45% Sodium Chloride 1,000 mL Bag

image description

OXYTOCIN 
oxytocin injection, solution
Product Information
Product TypeHUMAN PRESCRIPTION DRUGItem Code (Source)NDC:52533-234
Route of AdministrationINTRAVENOUS
Active Ingredient/Active Moiety
Ingredient NameBasis of StrengthStrength
OXYTOCIN (UNII: 1JQS135EYN) (OXYTOCIN - UNII:1JQS135EYN) OXYTOCIN30 [USP'U]  in 1000 mL
Inactive Ingredients
Ingredient NameStrength
DEXTROSE MONOHYDRATE (UNII: LX22YL083G) 50 g  in 1000 mL
SODIUM CHLORIDE (UNII: 451W47IQ8X) 4.5 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:52533-234-241000 mL in 1 BAG; Type 0: Not a Combination Product
Marketing Information
Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
unapproved drug other03/18/2016
Labeler - Cantrell Drug Company (035545763)

Revised: 3/2016
Document Id: d7c0695e-70ad-4a5c-b2a3-55834bab1f1a
Set id: c7a56694-0314-4b2d-965e-c665e7453e5b
Version: 1
Effective Time: 20160318
 
Cantrell Drug Company