Your browser does not support JavaScript! OXYTOCIN INJECTION, SOLUTION [CANTRELL DRUG COMPANY]
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RxNorm Names

OXYTOCIN injection, solution
[Cantrell Drug Company]


Category DEA Schedule Marketing Status
HUMAN PRESCRIPTION DRUG LABEL unapproved drug other
NOTE: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.
Drug Label Sections

Label

Label

OXYTOCIN 
oxytocin injection, solution
Product Information
Product TypeHUMAN PRESCRIPTION DRUG LABELItem Code (Source)NDC:52533-051
Route of AdministrationINTRAVENOUSDEA Schedule    
Active Ingredient/Active Moiety
Ingredient NameBasis of StrengthStrength
OXYTOCIN (OXYTOCIN) OXYTOCIN10 [USP'U]  in 500 mL
Inactive Ingredients
Ingredient NameStrength
SODIUM CHLORIDE3 g  in 500 mL
SODIUM LACTATE1.55 g  in 500 mL
POTASSIUM CHLORIDE0.15 g  in 500 mL
CALCIUM CHLORIDE0.1 g  in 500 mL
WATER 
Packaging
#Item CodePackage Description
1NDC:52533-051-29500 mL in 1 BAG
Marketing Information
Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
unapproved drug other11/12/2012
Labeler - Cantrell Drug Company (035545763)

Revised: 11/2012
Document Id: 3f071d89-76e4-4313-8e37-61c524758737
Set id: 238a22e0-37e9-4cc6-8612-c226d56a5d62
Version: 1
Effective Time: 20121112
 
Cantrell Drug Company

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