Potassium Chloride

Product NDC
58118-1526
11-digit product format
581181526
Labeler code
58118
Product ID
58118-1526_b02680e2-2286-73b9-e053-2a95a90aa899
Type
HUMAN PRESCRIPTION DRUG
Nonproprietary name
Potassium Chloride
Dosage form
TABLET, FILM COATED, EXTENDED RELEASE
Route
ORAL
Labeler
Clinical Solutions Wholesale
Application
NDA019123
Marketing category
NDA
Marketing start
1986-04-17
Marketing end
0000-00-00
Substance
POTASSIUM CHLORIDE
Active strength
750 mg/1
Pharmacologic classes
Potassium Compounds [CS],Potassium Salt [EPC],Osmotic Laxative [EPC],Increased Large Intestinal Motility [PE],Inhibition Large Intestine Fluid/Electrolyte Absorption [PE],Osmotic Activity [MoA]
NDC exclude flag
No
Listing certified through
2021-12-31
Current FDA listing
Historical FDA.report record

FDA-Initiated Inactive NDC Indexing#

DailyMed Socrata Ingredients#

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDCDashboard titleSPL versionValidationDashboard ZIP
58118-1526POTASSIUM CHLORIDE TABLET, FILM COATED, EXTENDED RELEASE [CLINICAL SOLUTIONS WHOLESALE]9Legacy NDC20200926_850b5b94-05a7-468c-8b90-77a1d45cd5c1.zip

Packages#

Package NDC, 11-digit format, Description table
Package NDC11-digit formatDescriptionMarketing startMarketing endSampleExclude flagStatus
58118-1526-85811815260830 TABLET, FILM COATED, EXTENDED RELEASE in 1 BLISTER PACK (58118-1526-8) 1986-04-170000-00-00NoNoCurrent