Label: MORPHINE SULFATE injection, solution
- NDC Code(s): 52533-137-12
- Packager: Cantrell Drug Company
- Category: HUMAN PRESCRIPTION DRUG LABEL
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Updated May 2, 2014
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INGREDIENTS AND APPEARANCE
morphine sulfate injection, solution
Product Information Product Type HUMAN PRESCRIPTION DRUG Item Code (Source) NDC:52533-137 Route of Administration INTRAVENOUS, INTRATHECAL DEA Schedule CII Active Ingredient/Active Moiety Ingredient Name Basis of Strength Strength MORPHINE SULFATE (UNII: X3P646A2J0) (MORPHINE - UNII:76I7G6D29C) MORPHINE SULFATE 0.5 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:52533-137-12 10 mL in 1 SYRINGE, PLASTIC Marketing Information Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date unapproved drug other 01/23/2012 Labeler - Cantrell Drug Company (035545763)