Potassium Acetate
POTASSIUM ACETATEInjection, USP
Approved
Approval ID
8123cce8-42e3-49e4-a488-3bb836ecccd0
Product Type
HUMAN PRESCRIPTION DRUG LABEL
Effective Date
Dec 4, 2019
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 DateDecember 4, 2019
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