Klor-Con

Product NDC
55289-697
11-digit product format
552890697
Labeler code
55289
Product ID
55289-697_7b32d2b6-3f09-7777-e053-2991aa0a18a1
Type
HUMAN PRESCRIPTION DRUG
Nonproprietary name
Potassium Chloride
Dosage form
TABLET, FILM COATED, EXTENDED RELEASE
Route
ORAL
Labeler
PD-Rx Pharmaceuticals, Inc.
Application
NDA019123
Marketing category
NDA
Marketing start
1986-04-17
Marketing end
0000-00-00
Substance
POTASSIUM CHLORIDE
Active strength
600 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
55289-697-30EA - Each55289-6971cb9d568-4f7a-49e0-b224-7f504d5ff9a012012-07-24
55289-697-90EA - Each55289-697445be466-abac-4ec8-8523-e0a1f80d67b812012-07-24