NOREPINEPHRINE BITARTRATE - norepinephrine bitartrate 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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Norepinephrine Bitartrate 4 mg Added to 5% Dextrose 250 mL Bag

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 
Other Ingredients
Ingredient KindIngredient NameQuantity
May containHYDROCHLORIC ACID 
May containSODIUM HYDROXIDE 
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: 12/2014
Document Id: 39eaa55c-765d-4e64-b1d7-9ad219f85c70
Set id: 62c8f853-8052-4558-97c7-55637d82eb1a
Version: 7
Effective Time: 20141224
 
Cantrell Drug Company