MORPHINE SULFATE - morphine sulfate 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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Morphine Sulfate 1 mg/mL in 0.9% Sodium Chloride 30 mL Syringe

MM1

MORPHINE SULFATE 
morphine sulfate injection, solution
Product Information
Product Type HUMAN PRESCRIPTION DRUG Item Code (Source) NDC:52533-160
Route of Administration INTRAVENOUS DEA Schedule CII    
Active Ingredient/Active Moiety
Ingredient Name Basis of Strength Strength
MORPHINE SULFATE (UNII: X3P646A2J0) (MORPHINE - UNII:76I7G6D29C) MORPHINE SULFATE 1 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:52533-160-03 30 mL in 1 SYRINGE, PLASTIC
Marketing Information
Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date
unapproved drug other 08/16/2012
Labeler - Cantrell Drug Company (035545763)

Revised: 4/2014
Document Id: bbf9bd2f-f34e-4fe9-bd8b-9c84a9173550
Set id: 74b2a815-7751-4c82-8fa7-9f29746940d5
Version: 4
Effective Time: 20140430
 
Cantrell Drug Company