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FDA Approval

Morphine Sulfate

Company

Cantrell Drug Company (DUNS: 035545763)

Effective Date

October 20, 2014

Labeling Type

HUMAN PRESCRIPTION DRUG LABEL

Active Ingredients

Morphine(1 mg in 1 mL)

Products (1)

Morphine Sulfate

NDC Product Code

52533-059

Route of Administration

INTRAVENOUS

Effective Date

October 20, 2014

Ingredients

Code: X3P646A2J0Class: ACTIBQuantity: 1 mg in 1 mL

DEXTROSEInactive

Code: IY9XDZ35W2Class: IACTQuantity: 5 g in 1 mL

WaterInactive

Code: 059QF0KO0RClass: IACT

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