Potassium Chloride

Product NDC
0615-8318
11-digit product format
006158318
Labeler code
0615
Product ID
0615-8318_32979e9e-e084-4693-abdd-adb178c19da6
Type
HUMAN PRESCRIPTION DRUG
Nonproprietary name
potassium chloride
Dosage form
TABLET, FILM COATED, EXTENDED RELEASE
Route
ORAL
Labeler
NCS HealthCare of KY, Inc dba Vangard Labs
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
2020-12-31
Current FDA listing
Historical FDA.report record

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDCDashboard titleSPL versionValidationDashboard ZIP
0615-8318POTASSIUM CHLORIDE TABLET, FILM COATED, EXTENDED RELEASE [NCS HEALTHCARE OF KY, LLC DBA VANGARD LABS]3Legacy NDC20241207_e3fad0ed-6c46-4555-a0b0-8cbb4f5b99e1.zip

Packages#

Package NDC, 11-digit format, Description table
Package NDC11-digit formatDescriptionMarketing startMarketing endSampleExclude flagStatus
0615-8318-050061583180515 TABLET, FILM COATED, EXTENDED RELEASE in 1 BLISTER PACK (0615-8318-05) 2019-09-300000-00-00NoNoCurrent
0615-8318-140061583181414 TABLET, FILM COATED, EXTENDED RELEASE in 1 BLISTER PACK (0615-8318-14) 2019-09-300000-00-00NoNoCurrent
0615-8318-390061583183930 TABLET, FILM COATED, EXTENDED RELEASE in 1 BLISTER PACK (0615-8318-39) 2019-09-300000-00-00NoNoCurrent