Potassium Acetate
Potassium Acetate Injection USP
Approved
Approval ID
c7eabefd-2781-439b-b8f4-cb3ea25a4720
Product Type
HUMAN PRESCRIPTION DRUG LABEL
Effective Date
Jul 20, 2021
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.
POTASSIUM ACETATE
Product Details
FDA regulatory identification and product classification information
FDA Identifiers
NDC Product Code0409-8183
Application NumberNDA018896
Product Classification
M
Marketing Category
C73594
G
Generic Name
POTASSIUM ACETATE
Product Specifications
Route of AdministrationINTRAVENOUS
Effective DateJuly 20, 2021
FDA Product Classification
INGREDIENTS (3)
POTASSIUM ACETATEActive
Quantity: 3.93 g in 20 mL
Code: M911911U02
Classification: ACTIB
WATERInactive
Code: 059QF0KO0R
Classification: IACT
ACETIC ACIDInactive
Code: Q40Q9N063P
Classification: IACT