Sodium Bicarbonate
Sodium Bicarbonate Injection, USP
Approved
Approval ID
e4ef2cb3-3d80-4d71-b50f-15571caac73a
Product Type
HUMAN PRESCRIPTION DRUG LABEL
Effective Date
Jan 19, 2024
Manufacturers
FDA
Hospira, Inc.
DUNS: 141588017
Products 1
Detailed information about drug products covered under this FDA approval, including NDC codes, dosage forms, ingredients, and administration routes.
SODIUM BICARBONATE
Product Details
FDA regulatory identification and product classification information
FDA Identifiers
NDC Product Code0409-4900
Application NumberANDA202495
Product Classification
M
Marketing Category
C73584
G
Generic Name
SODIUM BICARBONATE
Product Specifications
Route of AdministrationINTRAVENOUS
Effective DateJanuary 19, 2024
FDA Product Classification
INGREDIENTS (2)
SODIUM BICARBONATEActive
Quantity: 84 mg in 1 mL
Code: 8MDF5V39QO
Classification: ACTIB
WATERInactive
Code: 059QF0KO0R
Classification: IACT