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

OXYTOCIN 
oxytocin injection, solution
Product Information
Product TypeHUMAN PRESCRIPTION DRUG LABELItem Code (Source)NDC:52533-105
Route of AdministrationINTRAVENOUSDEA Schedule    
Active Ingredient/Active Moiety
Ingredient NameBasis of StrengthStrength
OXYTOCIN (OXYTOCIN) OXYTOCIN2 [USP'U]  in 100 mL
Inactive Ingredients
Ingredient NameStrength
WATER 
SODIUM CHLORIDE600 mg  in 100 mL
SODIUM LACTATE310 mg  in 100 mL
POTASSIUM CHLORIDE30 mg  in 100 mL
CALCIUM CHLORIDE20 mg  in 100 mL
DEXTROSE MONOHYDRATE5 g  in 100 mL
Packaging
#Item CodePackage DescriptionMarketing Start DateMarketing End Date
1NDC:52533-105-441000 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: 5/2013
 
Cantrell Drug Company

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