Potassium Chloride

Product NDC
0615-8337
11-digit product format
006158337
Labeler code
0615
Product ID
0615-8337_8f5d13e7-80e1-4764-917c-5eaf0afa556e
Type
HUMAN PRESCRIPTION DRUG
Nonproprietary name
Potassium Chloride
Dosage form
TABLET, EXTENDED RELEASE
Route
ORAL
Labeler
NCS HealthCare of KY, LLC dba Vangard Labs
Application
ANDA206347
Marketing category
ANDA
Marketing start
2016-01-21
Marketing end
2022-07-31
Substance
POTASSIUM CHLORIDE
Active strength
20 meq/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
0000-00-00
Current FDA listing
Historical FDA.report record

Packages#

Package NDC, 11-digit format, Description table
Package NDC11-digit formatDescriptionUnitsMarketing startMarketing endSampleExclude flagStatus
0615-8337-050061583370515 TABLET, EXTENDED RELEASE in 1 BLISTER PACK (0615-8337-05) 2020-05-270000-00-00NoNoCurrent
0615-8337-30006158337306 BLISTER PACK in 1 BOX, UNIT-DOSE (0615-8337-30) > 5 TABLET, EXTENDED RELEASE in 1 BLISTER PACK6 blister pack2020-05-260000-00-00NoNoCurrent
0615-8337-390061583373930 TABLET, EXTENDED RELEASE in 1 BLISTER PACK (0615-8337-39) 2020-05-270000-00-00NoNoCurrent