Morphine Sulfate
Morphine Sulfate 2 mg/mL in 0.9% Sodium Chloride Syringe
Approved
Approval ID
d2f9f46e-c3f6-4926-a72c-c24c9f1510e0
Product Type
HUMAN PRESCRIPTION DRUG LABEL
Effective Date
May 2, 2014
Manufacturers
FDA
Cantrell Drug Company
DUNS: 035545763
Products 1
Detailed information about drug products covered under this FDA approval, including NDC codes, dosage forms, ingredients, and administration routes.
Morphine Sulfate
Product Details
FDA regulatory identification and product classification information
FDA Identifiers
NDC Product Code52533-161
Product Classification
G
Generic Name
Morphine Sulfate
Product Specifications
Route of AdministrationINTRAVENOUS, INTRAMUSCULAR, INTRATHECAL, EPIDURAL
Effective DateMay 1, 2014
FDA Product Classification
INGREDIENTS (5)
Morphine SulfateActive
Quantity: 2 mg in 1 mL
Code: X3P646A2J0
Classification: ACTIB
WaterInactive
Code: 059QF0KO0R
Classification: IACT
SODIUM HYDROXIDEInactive
Code: 55X04QC32I
Classification: CNTM
Sodium ChlorideInactive
Quantity: 9 mg in 1 mL
Code: 451W47IQ8X
Classification: IACT
SULFURIC ACIDInactive
Code: O40UQP6WCF
Classification: CNTM