Klor-Con

Product NDC
67544-237
11-digit product format
675440237
Labeler code
67544
Product ID
67544-237_c3fb8c8c-fa8d-4890-a843-1999add4d22b
Type
HUMAN PRESCRIPTION DRUG
Nonproprietary name
Potassium Chloride
Dosage form
TABLET, FILM COATED, EXTENDED RELEASE
Route
ORAL
Labeler
Aphena Pharma Solutions - Tennessee, LLC
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
2019-12-31
Current FDA listing
Historical FDA.report record

DailyMed Billing Units#

Package NDC, Billing unit, Product NDC table
Package NDCBilling unitProduct NDCDailyMed indexing SPLSPL versionEffective
67544-237-30EA - Each67544-2375e8820e2-1665-4fea-a377-412605e1582512014-06-03
67544-237-53EA - Each67544-237bbf696aa-f9d0-474a-8a18-ceb515f6f1b212014-06-03
67544-237-60EA - Each67544-237b97d9059-7ed6-4f1b-917f-34d6ada9e4cd12013-06-04
67544-237-70EA - Each67544-2375901ae8a-7458-44f9-8b57-0997f7238ff312014-06-03
67544-237-80EA - Each67544-237b5ee4d97-75d2-4e97-86d4-ae2aaa20d17312013-06-04
67544-237-92EA - Each67544-2374bbfb7f5-2306-4408-801e-4a19750474a712014-06-03
67544-237-94EA - Each67544-237d6242e05-a12c-423d-9c4f-aa4a982014ea12013-06-04