Sodium Bicarbonate
SODIUM BICARBONATE Injection, USP
Approved
Approval ID
2a262fe3-8a64-4dc5-954a-1d51fb72747b
Product Type
HUMAN PRESCRIPTION DRUG LABEL
Effective Date
Jul 3, 2014
Manufacturers
FDA
US MedSource, LLC
DUNS: 032793851
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 Code61699-6625
Product Classification
G
Generic Name
SODIUM BICARBONATE
Product Specifications
Route of AdministrationINTRAVENOUS
Effective DateJuly 2, 2014
FDA Product Classification
INGREDIENTS (2)
SODIUM BICARBONATEActive
Quantity: 84 mg in 1 mL
Code: 8MDF5V39QO
Classification: ACTIB
WATERInactive
Code: 059QF0KO0R
Classification: IACT