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 20 USP Units Added to 0.9% Sodium Chloride 1000 mL Bag

image description

OXYTOCIN 
oxytocin injection, solution
Product Information
Product TypeHUMAN PRESCRIPTION DRUGItem Code (Source)NDC:52533-050
Route of AdministrationINTRAVENOUS
Active Ingredient/Active Moiety
Ingredient NameBasis of StrengthStrength
OXYTOCIN (UNII: 1JQS135EYN) (OXYTOCIN - UNII:1JQS135EYN) OXYTOCIN20 [USP'U]  in 1000 mL
Inactive Ingredients
Ingredient NameStrength
SODIUM CHLORIDE (UNII: 451W47IQ8X) 9 g  in 1000 mL
WATER (UNII: 059QF0KO0R)  
Packaging
#Item CodePackage DescriptionMarketing Start DateMarketing End Date
1NDC:52533-050-241000 mL in 1 BAG; Type 0: Not a Combination Product10/20/201112/06/2017
Marketing Information
Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
unapproved drug other10/20/201112/06/2017
Labeler - Cantrell Drug Company (035545763)

Revised: 12/2017
Document Id: 5fae7621-3c3f-7708-e053-2991aa0a2582
Set id: 32ab2505-9bb7-49d6-af24-ec95c8edfa8b
Version: 6
Effective Time: 20171206
 
Cantrell Drug Company