Your browser does not support JavaScript! HEPARIN SODIUM INJECTION, SOLUTION [CANTRELL DRUG COMPANY]
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RxNorm Names

HEPARIN SODIUM 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

HEPARIN SODIUM 
heparin sodium injection, solution
Product Information
Product TypeHUMAN PRESCRIPTION DRUG LABELItem Code (Source)NDC:52533-125
Route of AdministrationINTRAVENOUSDEA Schedule    
Active Ingredient/Active Moiety
Ingredient NameBasis of StrengthStrength
Heparin Sodium (Heparin) Heparin Sodium4 [USP'U]  in 1 mL
Inactive Ingredients
Ingredient NameStrength
Sodium Chloride9 mg  in 1 mL
BENZYL ALCOHOL0.00004 mL  in 1 mL
Water 
Packaging
#Item CodePackage Description
1NDC:52533-125-241000 mL in 1 BAG
Marketing Information
Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
unapproved drug other05/09/2012
Labeler - Cantrell Drug Company (035545763)

Revised: 12/2012
Document Id: 7d4e6092-e878-401d-b15e-a36eace87cca
Set id: 93ffe3f7-26bf-44e5-be3c-1dd58abb1066
Version: 4
Effective Time: 20121203
 
Cantrell Drug Company

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