Potassium Chloride
POTASSIUM CHLORIDE EXTENDED-RELEASE CAPSULES, USP, 8 mEq and 10 mEq
Approved
Approval ID
01d29de1-d6e7-4e99-ba77-83c26caba597
Product Type
HUMAN PRESCRIPTION DRUG LABEL
Effective Date
Jul 6, 2017
Manufacturers
FDA
Carilion Materials Management
DUNS: 079239644
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
NDC Product Code68151-0609
Application NumberANDA077419
Marketing CategoryC73584
Route of AdministrationORAL
Effective DateMay 20, 2015
Generic NamePotassium Chloride
INGREDIENTS (6)
POTASSIUM CHLORIDEActive
Quantity: 600 mg in 1 1
Code: 660YQ98I10
Classification: ACTIB
ETHYLCELLULOSE, UNSPECIFIEDInactive
Code: 7Z8S9VYZ4B
Classification: IACT
SODIUM LAURYL SULFATEInactive
Code: 368GB5141J
Classification: IACT
TRIACETINInactive
Code: XHX3C3X673
Classification: IACT
TITANIUM DIOXIDEInactive
Code: 15FIX9V2JP
Classification: IACT
GELATIN, UNSPECIFIEDInactive
Code: 2G86QN327L
Classification: IACT