Sodium Bicarbonate
Sodium Bicarbonate Injection, USP
Approved
Approval ID
09cf38c2-0b44-eca1-e063-6294a90a72d8
Product Type
HUMAN PRESCRIPTION DRUG LABEL
Effective Date
Nov 10, 2023
Manufacturers
FDA
Medical Purchasing Solutions, LLC
DUNS: 601458529
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 Code71872-7310
Application NumberANDA211091
Product Classification
M
Marketing Category
C73584
G
Generic Name
SODIUM BICARBONATE
Product Specifications
Route of AdministrationINTRAVENOUS
Effective DateNovember 10, 2023
FDA Product Classification
INGREDIENTS (2)
WATERInactive
Code: 059QF0KO0R
Classification: IACT
SODIUM BICARBONATEActive
Quantity: 84 mg in 1 mL
Code: 8MDF5V39QO
Classification: ACTIB