Hydromorphone HCl 0.5 mg/mL in 0.9% Sodium Chloride 1 mL Syringe

HYDROMORPHONE HCL - hydromorphone hcl 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
hydromorphone hcl injection, solution

Product Information
Product Type	HUMAN PRESCRIPTION DRUG	Item Code (Source)	NDC:52533-005
Route of Administration	INTRAVENOUS, INTRAMUSCULAR, SUBCUTANEOUS	DEA Schedule	CII

Ingredient Name	Basis of Strength	Strength
Active Ingredient/Active Moiety
HYDROMORPHONE HYDROCHLORIDE (UNII: L960UP2KRW) (HYDROMORPHONE - UNII:Q812464R06)	HYDROMORPHONE HYDROCHLORIDE	0.5 mg in 1 mL

Ingredient Kind	Ingredient Name	Quantity
Other Ingredients
May contain	HYDROCHLORIC ACID (UNII: QTT17582CB)
May contain	SODIUM HYDROXIDE (UNII: 55X04QC32I)

#	Item Code	Package Description	Marketing Start Date	Marketing End Date
Packaging
1	NDC:52533-005-45	1 mL in 1 SYRINGE, PLASTIC

Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
Marketing Information
unapproved drug other		10/11/2013

Labeler - Cantrell Drug Company (035545763)