Magnesium Sulfate
Magnesium Sulfate
Approved
Approval ID
5176ed24-015e-43fe-9eb4-85098debf5f1
Product Type
HUMAN PRESCRIPTION DRUG LABEL
Effective Date
Nov 9, 2023
Manufacturers
FDA
Henry Schein, Inc.
DUNS: 012430880
Products 1
Detailed information about drug products covered under this FDA approval, including NDC codes, dosage forms, ingredients, and administration routes.
Magnesium Sulfate
Product Details
FDA regulatory identification and product classification information
FDA Identifiers
NDC Product Code0404-9904
Application NumberNDA019316
Product Classification
M
Marketing Category
C73594
G
Generic Name
Magnesium Sulfate
Product Specifications
Route of AdministrationINTRAMUSCULAR, INTRAVENOUS
Effective DateNovember 9, 2023
FDA Product Classification
INGREDIENTS (3)
SULFURIC ACIDInactive
Code: O40UQP6WCF
Classification: IACT
SODIUM HYDROXIDEInactive
Code: 55X04QC32I
Classification: IACT
MAGNESIUM SULFATE HEPTAHYDRATEActive
Quantity: 500 mg in 1 mL
Code: SK47B8698T
Classification: ACTIB