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

HYDROMORPHONE 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

HYDROMORPHONE HCL 
hydromorphone hcl injection, solution
Product Information
Product TypeHUMAN PRESCRIPTION DRUG LABELItem Code (Source)NDC:52533-002
Route of AdministrationINTRAVENOUSDEA ScheduleCII    
Active Ingredient/Active Moiety
Ingredient NameBasis of StrengthStrength
HYDROMORPHONE HYDROCHLORIDE (HYDROMORPHONE) HYDROMORPHONE HYDROCHLORIDE0.2 mg  in 1 mL
Inactive Ingredients
Ingredient NameStrength
Sodium Chloride9 mg  in 1 mL
WATER 
Packaging
#Item CodePackage Description
1NDC:52533-002-0530 mL in 1 VIAL, GLASS
Marketing Information
Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
unapproved drug other08/23/2010
Labeler - Cantrell Drug Company (035545763)

Revised: 05/2013
Document Id: 0c084d90-4158-4446-8bc9-6aa05522d73c
Set id: ac0d4ad4-a265-4690-bdfe-ab27b64e6b97
Version: 5
Effective Time: 20130501
 
Cantrell Drug Company

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