MORPHINE SULFATE injection, solution

Morphine Sulfate by

Drug Labeling and Warnings

Morphine Sulfate by is a Prescription medication manufactured, distributed, or labeled by Cantrell Drug Company. Drug facts, warnings, and ingredients follow.

Drug Details [pdf]

PRINCIPAL DISPLAY PANEL

SPL UNCLASSIFIED SECTION

INGREDIENTS AND APPEARANCE

MORPHINE SULFATE 
morphine sulfate injection, solution

Product Information
Product Type	HUMAN PRESCRIPTION DRUG	Item Code (Source)	NDC: 52533-161
Route of Administration	INTRAVENOUS, INTRAMUSCULAR, INTRATHECAL, EPIDURAL	DEA Schedule	CII

Active Ingredient/Active Moiety
Ingredient Name	Basis of Strength	Strength
Morphine Sulfate (UNII: X3P646A2J0) (Morphine - UNII:76I7G6D29C)	Morphine Sulfate	2 mg  in 1 mL

Inactive Ingredients
Ingredient Name	Strength
Sodium Chloride (UNII: 451W47IQ8X)	9 mg  in 1 mL
Water (UNII: 059QF0KO0R)

Other Ingredients
Ingredient Kind	Ingredient Name	Quantity
May contain	SULFURIC ACID (UNII: O40UQP6WCF)
May contain	SODIUM HYDROXIDE (UNII: 55X04QC32I)

Packaging
#	Item Code	Package Description	Marketing Start Date	Marketing End Date
1	NDC: 52533-161-45	1 mL in 1 SYRINGE, PLASTIC

Marketing Information
Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
unapproved drug other		02/22/2012

Labeler - Cantrell Drug Company (035545763)