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Morphine Sulfate

Morphine Sulfate 5 mg/mL in 0.9% Sodium Chloride 30 mL Monoject Syringe Barrel

Approved
Approval ID

093bee1a-a532-4dc1-83df-c0c5c7cdc58a

Product Type

HUMAN PRESCRIPTION DRUG LABEL

Effective Date

Apr 30, 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 Code52533-132
Product Classification
G
Generic Name
Morphine Sulfate
Product Specifications
Route of AdministrationINTRAVENOUS
Effective DateApril 28, 2014
FDA Product Classification

INGREDIENTS (5)

Sodium ChlorideInactive
Quantity: 9 mg in 1 mL
Code: 451W47IQ8X
Classification: IACT
MORPHINE SULFATEActive
Quantity: 5 mg in 1 mL
Code: X3P646A2J0
Classification: ACTIB
WaterInactive
Code: 059QF0KO0R
Classification: IACT
SULFURIC ACIDInactive
Code: O40UQP6WCF
Classification: CNTM
SODIUM HYDROXIDEInactive
Code: 55X04QC32I
Classification: CNTM

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Morphine Sulfate - FDA Drug Approval Details