Potassium Acetate
Potassium Acetate Injection USP
Approved
Approval ID
a9485880-933d-4f82-9728-22397126a1d4
Product Type
HUMAN PRESCRIPTION DRUG LABEL
Effective Date
Jan 7, 2016
Manufacturers
FDA
Exela Pharma Sciences, LLC
DUNS: 831274399
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 Code51754-2001
Application NumberANDA206203
Product Classification
M
Marketing Category
C73584
G
Generic Name
POTASSIUM ACETATE
Product Specifications
Route of AdministrationINTRAVENOUS
Effective DateJanuary 7, 2016
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