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

NOREPINEPHRINE BITARTRATE 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

NOREPINEPHRINE BITARTRATE 
norepinephrine bitartrate injection, solution
Product Information
Product TypeHUMAN PRESCRIPTION DRUG LABELItem Code (Source)NDC:52533-165
Route of AdministrationINTRAVENOUSDEA Schedule    
Active Ingredient/Active Moiety
Ingredient NameBasis of StrengthStrength
Norepinephrine Bitartrate (Norepinephrine) Norepinephrine16 ug  in 1 mL
Inactive Ingredients
Ingredient NameStrength
Dextrose50 mg  in 1 mL
Water 
Packaging
#Item CodePackage DescriptionMarketing Start DateMarketing End Date
1NDC:52533-165-38250 mL in 1 BAG
Marketing Information
Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
unapproved drug other04/12/2012
Labeler - Cantrell Drug Company (035545763)

Revised: 11/2013
 
Cantrell Drug Company

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