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

Label

Label

PHENYLEPHRINE HCL 
phenylephrine hcl injection, solution
Product Information
Product TypeHUMAN PRESCRIPTION DRUG LABELItem Code (Source)NDC:52533-171
Route of AdministrationINTRAVENOUSDEA Schedule    
Active Ingredient/Active Moiety
Ingredient NameBasis of StrengthStrength
Phenylephrine Hydrochloride (Phenylephrine) Phenylephrine Hydrochloride100 ug  in 1 mL
Inactive Ingredients
Ingredient NameStrength
Sodium Chloride9 mg  in 1 mL
Water 
Packaging
#Item CodePackage Description
1NDC:52533-171-1210 mL in 1 SYRINGE, PLASTIC
Marketing Information
Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
unapproved drug other08/30/2012
Labeler - Cantrell Drug Company (035545763)

Revised: 03/2013
Document Id: d98ec319-b75b-45dd-bd50-5963b6fc20c8
Set id: 20562220-5425-4eb4-9b52-52851f8c9977
Version: 4
Effective Time: 20130305
 
Cantrell Drug Company

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