sodium chloride
0.45% Sodium Chloride Injection, USP
Approved
Approval ID
8df7dcf6-8714-6caf-e053-2995a90ab8cc
Product Type
HUMAN PRESCRIPTION DRUG LABEL
Effective Date
Jul 18, 2019
Manufacturers
FDA
Becton Dickinson and Company
DUNS: 124987988
Products 1
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 Code17271-700
Application NumberANDA208122
Product Classification
M
Marketing Category
C73584
G
Generic Name
SODIUM CHLORIDE
Product Specifications
Route of AdministrationINTRAVENOUS
Effective DateJuly 18, 2019
FDA Product Classification
INGREDIENTS (2)
WATERInactive
Code: 059QF0KO0R
Classification: IACT
SODIUM CHLORIDEActive
Quantity: 450 mg in 100 mL
Code: 451W47IQ8X
Classification: ACTIB