3% Sodium Chloride
3% Sodium Chloride Injection, USP
Approved
Approval ID
a8058593-48af-457a-b0f0-166935c7d10c
Product Type
HUMAN PRESCRIPTION DRUG LABEL
Effective Date
Jan 14, 2021
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.
3% Sodium Chloride
Product Details
FDA regulatory identification and product classification information
FDA Identifiers
NDC Product Code17271-703
Application NumberANDA209476
Product Classification
M
Marketing Category
C73584
G
Generic Name
3% Sodium Chloride
Product Specifications
Route of AdministrationINTRAVENOUS
Effective DateFebruary 27, 2020
FDA Product Classification
INGREDIENTS (3)
SODIUM CHLORIDEActive
Quantity: 3 g in 100 mL
Code: 451W47IQ8X
Classification: ACTIB
WATERInactive
Code: 059QF0KO0R
Classification: IACT
HYDROCHLORIC ACIDInactive
Code: QTT17582CB
Classification: IACT