Klor-Con

Product NDC
0440-8110
11-digit product format
004408110
Labeler code
0440
Product ID
0440-8110_2cbf8674-25ac-4009-9bb6-89ca9b3b3317
Type
HUMAN PRESCRIPTION DRUG
Nonproprietary name
Potassium Chloride
Dosage form
TABLET, FILM COATED, EXTENDED RELEASE
Route
ORAL
Labeler
Liberty Pharmaceuticals, Inc.
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 Billing Units#

Package NDC, Billing unit, Product NDC table
Package NDCBilling unitProduct NDCDailyMed indexing SPLSPL versionEffective
0440-8110-92EA - Each0440-81104e3b247a-470c-4ca8-b32e-5a4137442f3012013-10-17