HYDROMORPHONE HCL - hydromorphone hydrochloride injection, solution 
Cantrell Drug Company

Disclaimer: 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.

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Hydromorphone HCl 1 mg/mL in 0.9% Sodium Chloride 30 mL Monoject Syringe Barrel

Label

Label

HYDROMORPHONE HCL 
hydromorphone hcl injection, solution
Product Information
Product TypeHUMAN PRESCRIPTION DRUG LABELItem Code (Source)NDC:52533-006
Route of AdministrationINTRAVENOUSDEA ScheduleCII    
Active Ingredient/Active Moiety
Ingredient NameBasis of StrengthStrength
HYDROMORPHONE HYDROCHLORIDE (HYDROMORPHONE) HYDROMORPHONE HYDROCHLORIDE1 mg  in 1 mL
Inactive Ingredients
Ingredient NameStrength
Sodium Chloride9 mg  in 1 mL
WATER 
Other Ingredients
Ingredient KindIngredient NameQuantity
May containHYDROCHLORIC ACID 
May containSODIUM HYDROXIDE 
Packaging
#Item CodePackage DescriptionMarketing Start DateMarketing End Date
1NDC:52533-006-4830 mL in 1 SYRINGE, PLASTIC
Marketing Information
Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
unapproved drug other10/11/2013
Labeler - Cantrell Drug Company (035545763)

Revised: 4/2014
Document Id: ed4c353a-aa8f-470a-8018-ae34a5f06e00
Set id: daa5485b-8ee2-414b-9ed5-081bc7149ef5
Version: 4
Effective Time: 20140430
 
Cantrell Drug Company