Sodium Chloride
Sodium Chloride Injection
Approved
Approval ID
7e316d21-d6ad-4976-bd90-268fd7e51361
Product Type
HUMAN PRESCRIPTION DRUG LABEL
Effective Date
Jan 12, 2024
Manufacturers
FDA
Spectra Medical Deviecs, LLC
DUNS: 118301171
Products 2
Detailed information about drug products covered under this FDA approval, including NDC codes, dosage forms, ingredients, and administration routes.
Sodium Chloride
Product Details
FDA regulatory identification and product classification information
FDA Identifiers
NDC Product Code65282-1505
Application NumberANDA206171
Product Classification
M
Marketing Category
C73584
G
Generic Name
Sodium Chloride
Product Specifications
Route of AdministrationINTRAVENOUS, INTRAMUSCULAR, SUBCUTANEOUS
Effective DateJanuary 12, 2024
FDA Product Classification
INGREDIENTS (1)
SODIUM CHLORIDEActive
Quantity: 9 mg in 1 mL
Code: 451W47IQ8X
Classification: ACTIB
Sodium Chloride
Product Details
FDA regulatory identification and product classification information
FDA Identifiers
NDC Product Code65282-1510
Application NumberANDA206171
Product Classification
M
Marketing Category
C73584
G
Generic Name
Sodium Chloride
Product Specifications
Route of AdministrationINTRAMUSCULAR, INTRAVENOUS, SUBCUTANEOUS
Effective DateJanuary 12, 2024
FDA Product Classification
INGREDIENTS (1)
SODIUM CHLORIDEActive
Quantity: 9 mg in 1 mL
Code: 451W47IQ8X
Classification: ACTIB