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

MM1

HEPARIN SODIUM 
heparin sodium injection, solution
Product Information
Product TypeHUMAN PRESCRIPTION DRUG LABELItem Code (Source)NDC:52533-106
Route of AdministrationINTRAVENOUSDEA Schedule    
Active Ingredient/Active Moiety
Ingredient NameBasis of StrengthStrength
Heparin Sodium (Heparin) Heparin Sodium50 [USP'U]  in 1 mL
Inactive Ingredients
Ingredient NameStrength
DEXTROSE50 mg  in 1 mL
BENZYL ALCOHOL0.0001 mL  in 1 mL
Water 
Packaging
#Item CodePackage Description
1NDC:52533-106-32500 mL in 1 BAG
Marketing Information
Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
unapproved drug other08/09/2012
Labeler - Cantrell Drug Company (035545763)

Revised: 12/2012
Document Id: 5936746b-5d13-4501-9b8a-d0f0bc19a386
Set id: 49986fbc-5b4d-48b9-ace3-90182f53f6bb
Version: 5
Effective Time: 20121219
 
Cantrell Drug Company

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