Your browser does not support JavaScript! AMIODARONE HCL INJECTION, SOLUTION [CANTRELL DRUG COMPANY]
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AMIODARONE HCL 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

Preparation Label

AMIODARONE HCL 
amiodarone hcl injection, solution
Product Information
Product TypeHUMAN PRESCRIPTION DRUG LABELItem Code (Source)NDC:52533-101
Route of AdministrationINTRAVENOUSDEA Schedule    
Active Ingredient/Active Moiety
Ingredient NameBasis of StrengthStrength
AMIODARONE HYDROCHLORIDE (Amiodarone) AMIODARONE HYDROCHLORIDE1.8 mg  in 1 mL
Inactive Ingredients
Ingredient NameStrength
Dextrose50 mg  in 1 mL
POLYSORBATE 803.6 mg  in 1 mL
BENZYL ALCOHOL0.73 mg  in 1 mL
WATER 
Packaging
#Item CodePackage DescriptionMarketing Start DateMarketing End Date
1NDC:52533-101-59500 mL in 1 BAG
Marketing Information
Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
unapproved drug other10/18/2013
Labeler - Cantrell Drug Company (035545763)

Revised: 8/2014
 
Cantrell Drug Company

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