Your browser does not support JavaScript! MEPERIDINE HCL INJECTION, SOLUTION [CANTRELL DRUG COMPANY]
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MEPERIDINE HCL injection, solution
[Cantrell Drug Company]


Category DEA Schedule Marketing Status
HUMAN PRESCRIPTION DRUG LABEL CII 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

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MEPERIDINE HCL 
meperidine hcl injection, solution
Product Information
Product TypeHUMAN PRESCRIPTION DRUG LABELItem Code (Source)NDC:52533-042
Route of AdministrationINTRAVENOUSDEA ScheduleCII    
Active Ingredient/Active Moiety
Ingredient NameBasis of StrengthStrength
MEPERIDINE HYDROCHLORIDE (MEPERIDINE) MEPERIDINE HYDROCHLORIDE10 mg  in 1 mL
Inactive Ingredients
Ingredient NameStrength
Sodium Chloride9 mg  in 1 mL
WATER 
Packaging
#Item CodePackage Description
1NDC:52533-042-0450 mL in 1 SYRINGE, PLASTIC
Marketing Information
Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
unapproved drug other01/23/2012
Labeler - Cantrell Drug Company (035545763)
Establishment
NameAddressID/FEIBusiness Operations
Cantrell Drug Company035545763manufacture(52533-042)

Revised: 12/2012
Document Id: 78b64521-da5e-473c-9342-da1b6f16e1f5
Set id: 8c11ffb8-6ff6-473c-b613-e8936e161a00
Version: 3
Effective Time: 20121227
 
Cantrell Drug Company

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