Potassium Chloride
POTASSIUM CHLORIDE EXTENDED-RELEASE CAPSULES, USP, 10 mEq
Approved
Approval ID
94c1c765-7ede-419a-ad5a-fcaac8f67a8a
Product Type
HUMAN PRESCRIPTION DRUG LABEL
Effective Date
Feb 25, 2013
Manufacturers
FDA
Amneal Pharmaceuticals
DUNS: 123797875
Products 1
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 Code65162-542
Application NumberANDA202128
Product Classification
M
Marketing Category
C73584
G
Generic Name
Potassium Chloride
Product Specifications
Route of AdministrationORAL
Effective DateFebruary 25, 2013
FDA Product Classification
INGREDIENTS (5)
POTASSIUM CHLORIDEActive
Quantity: 750 mg in 1 1
Code: 660YQ98I10
Classification: ACTIB
ETHYLCELLULOSESInactive
Code: 7Z8S9VYZ4B
Classification: IACT
GELATINInactive
Code: 2G86QN327L
Classification: IACT
SODIUM LAURYL SULFATEInactive
Code: 368GB5141J
Classification: IACT
TRIETHYL CITRATEInactive
Code: 8Z96QXD6UM
Classification: IACT