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 8 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:52533-166
Route of AdministrationINTRAVENOUSDEA Schedule    
Active Ingredient/Active Moiety
Ingredient NameBasis of StrengthStrength
Norepinephrine Bitartrate (Norepinephrine) Norepinephrine32 ug  in 1 mL
Inactive Ingredients
Ingredient NameStrength
ANHYDROUS DEXTROSE50 mg  in 1 mL
SODIUM CHLORIDE236.8 ug  in 1 mL
SODIUM METABISULFITE64 ug  in 1 mL
WATER 
Other Ingredients
Ingredient KindIngredient NameQuantity
May containHYDROCHLORIC ACID 
May containSODIUM HYDROXIDE 
Packaging
#Item CodePackage DescriptionMarketing Start DateMarketing End Date
1NDC:52533-166-38250 mL in 1 BAG
Marketing Information
Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
unapproved drug other04/12/201203/06/2015
Labeler - Cantrell Drug Company (035545763)

Revised: 3/2015
Document Id: 11823c29-d91c-4b8c-94d4-e163e7a63ae1
Set id: 821d4d73-6cfc-4a82-a39e-5691caedc201
Version: 9
Effective Time: 20150306
 
Cantrell Drug Company