Potassium Chloride
Approved
Approval ID
8281fd53-f77b-42b1-9b90-449a504f5550
Product Type
HUMAN PRESCRIPTION DRUG LABEL
Effective Date
Sep 13, 2023
Manufacturers
FDA
Nexus Pharamaceuticals Inc.
DUNS: 620714787
Products 2
Detailed information about drug products covered under this FDA approval, including NDC codes, dosage forms, ingredients, and administration routes.
Potassium Chloride
Product Details
FDA regulatory identification and product classification information
FDA Identifiers
NDC Product Code14789-136
Application NumberANDA217704
Product Classification
M
Marketing Category
C73584
G
Generic Name
Potassium Chloride
Product Specifications
Route of AdministrationINTRAVENOUS
Effective DateSeptember 13, 2023
FDA Product Classification
INGREDIENTS (1)
Potassium ChlorideActive
Quantity: 29.8 mg in 1 mL
Code: 660YQ98I10
Classification: ACTIB
Potassium Chloride
Product Details
FDA regulatory identification and product classification information
FDA Identifiers
NDC Product Code14789-137
Application NumberANDA217704
Product Classification
M
Marketing Category
C73584
G
Generic Name
Potassium Chloride
Product Specifications
Route of AdministrationINTRAVENOUS
Effective DateSeptember 13, 2023
FDA Product Classification
INGREDIENTS (1)
Potassium ChlorideActive
Quantity: 29.8 mg in 1 mL
Code: 660YQ98I10
Classification: ACTIB