Morphine Sulfate

FDA-approved pharmaceutical product with comprehensive regulatory information, manufacturing details, and complete labeling documentation.

Company

Cantrell Drug Company

DUNS: 035545763

Effective Date

May 2, 2014

Labeling Type

HUMAN PRESCRIPTION DRUG LABEL

Active Ingredients

Morphine(2 mg in 1 mL)

Products1

Detailed information about drug products covered under this FDA approval, including NDC codes, dosage forms, ingredients, and administration routes.

NDC Product Code

52533-161

Route of Administration

INTRAVENOUS, INTRAMUSCULAR, INTRATHECAL, EPIDURAL

Effective Date

May 1, 2014

Ingredients

Code: X3P646A2J0Class: ACTIBQuantity: 2 mg in 1 mL

WaterInactive

Code: 059QF0KO0RClass: IACT

Code: 55X04QC32IClass: CNTM

Sodium ChlorideInactive

Code: 451W47IQ8XClass: IACTQuantity: 9 mg in 1 mL

Code: O40UQP6WCFClass: CNTM