Potassium Chloride
Potassium Chloride Extended-release Tablets, USP Microencapsulated
Approved
Approval ID
dbd309c5-7205-41e3-b8c4-cb06df375528
Product Type
HUMAN PRESCRIPTION DRUG LABEL
Effective Date
Aug 2, 2010
Manufacturers
FDA
Contract Pharmacy Services-PA
DUNS: 945429777
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 Code67046-590
Application NumberANDA074726
Product Classification
M
Marketing Category
C73584
G
Generic Name
Potassium Chloride
Product Specifications
Route of AdministrationORAL
Effective DateNovember 4, 2009
FDA Product Classification
INGREDIENTS (1)
POTASSIUM CHLORIDEActive
Quantity: 20 meq in 1 1
Code: 660YQ98I10
Classification: ACTIB
Potassium Chloride
Product Details
FDA regulatory identification and product classification information
FDA Identifiers
NDC Product Code67046-588
Application NumberANDA074726
Product Classification
M
Marketing Category
C73584
G
Generic Name
Potassium Chloride
Product Specifications
Route of AdministrationORAL
Effective DateNovember 4, 2009
FDA Product Classification
INGREDIENTS (1)
POTASSIUM CHLORIDEActive
Quantity: 10 meq in 1 1
Code: 660YQ98I10
Classification: ACTIB