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

LABETALOL HCL 
labetalol hcl injection, solution
Product Information
Product TypeHUMAN PRESCRIPTION DRUG LABELItem Code (Source)NDC:52533-034
Route of AdministrationINTRAVENOUSDEA Schedule    
Active Ingredient/Active Moiety
Ingredient NameBasis of StrengthStrength
LABETALOL HYDROCHLORIDE (LABETALOL) LABETALOL HYDROCHLORIDE5 mg  in 1 mL
Inactive Ingredients
Ingredient NameStrength
Water 
Anhydrous Dextrose45 mg  in 1 mL
Edetate Disodium0.1 mg  in 1 mL
Methylparaben0.8 mg  in 1 mL
Propylparaben0.1 mg  in 1 mL
Citric Acid Monohydrate 
Sodium Hydroxide 
Packaging
#Item CodePackage Description
1NDC:52533-034-204 mL in 1 SYRINGE, PLASTIC
Marketing Information
Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
unapproved drug other02/23/2012
Labeler - Cantrell Drug Company (035545763)

Revised: 11/2012
Document Id: a0214b06-2d2b-4203-8b19-070caef1a79f
Set id: f0a9df5b-45b5-4be5-aeb6-76d0c27a7799
Version: 2
Effective Time: 20121130
 
Cantrell Drug Company

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