Your browser does not support JavaScript! MAGNESIUM SULFATE INJECTION, SOLUTION [CANTRELL DRUG COMPANY]
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MAGNESIUM SULFATE 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

MAGNESIUM SULFATE 
magnesium sulfate injection, solution
Product Information
Product TypeHUMAN PRESCRIPTION DRUG LABELItem Code (Source)NDC:52533-099
Route of AdministrationINTRAVENOUSDEA Schedule    
Active Ingredient/Active Moiety
Ingredient NameBasis of StrengthStrength
MAGNESIUM SULFATE (Magnesium Cation) MAGNESIUM SULFATE20 g  in 500 mL
Inactive Ingredients
Ingredient NameStrength
WATER 
SODIUM CHLORIDE3 g  in 500 mL
SODIUM LACTATE1.55 g  in 500 mL
POTASSIUM CHLORIDE0.15 g  in 500 mL
CALCIUM CHLORIDE0.1 g  in 500 mL
Packaging
#Item CodePackage Description
1NDC:52533-099-29500 mL in 1 BAG
Marketing Information
Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
unapproved drug other02/21/2011
Labeler - Cantrell Drug Company (035545763)

Revised: 11/2012
Document Id: 6ff3505e-13ea-4bc8-a709-66b133c5a261
Set id: 88f80e1e-d6e3-4789-abe1-f62db9ca366b
Version: 2
Effective Time: 20121121
 
Cantrell Drug Company

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