Your browser does not support JavaScript! MAGNESIUM CHLORIDE INJECTION [MYLAN TEORANTA]
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RxNorm Names

MAGNESIUM CHLORIDE injection
[Mylan Teoranta]


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

      

      

  

PRINCIPAL DISPLAY PANEL - 200 mg/mL
NDC 67457-134-50     50 mL

Magnesium Chloride Injection 200 mg/mL (20 percent w/v) Carton Label
MAGNESIUM CHLORIDE 
magnesium chloride injection
Product Information
Product TypeHUMAN PRESCRIPTION DRUG LABELItem Code (Source)NDC:63286-0134
Route of AdministrationINTRAVENOUSDEA Schedule    
Active Ingredient/Active Moiety
Ingredient NameBasis of StrengthStrength
MAGNESIUM CHLORIDE (MAGNESIUM CATION) MAGNESIUM CHLORIDE200 mg  in 1 mL
Inactive Ingredients
Ingredient NameStrength
SODIUM CHLORIDE9 mg  in 1 mL
BENZYL ALCOHOL10 mg  in 1 mL
WATER 
HYDROCHLORIC ACID 
SODIUM HYDROXIDE 
Packaging
#Item CodePackage DescriptionMarketing Start DateMarketing End Date
1NDC:63286-0134-51 in 1 CARTON
150 mL in 1 VIAL, MULTI-DOSE
Marketing Information
Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
Unapproved drug other03/14/2013
Labeler - Mylan Teoranta (896321325)

Revised: 3/2013
 
Mylan Teoranta

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