Potassium Chloride

Product NDC
55154-8089
11-digit product format
551548089
Labeler code
55154
Product ID
55154-8089_f64a2b16-2e08-492a-8075-f838b93b7d70
Type
HUMAN PRESCRIPTION DRUG
Nonproprietary name
Potassium Chloride
Dosage form
CAPSULE, COATED, EXTENDED RELEASE
Route
ORAL
Labeler
Cardinal Health 107, LLC
Application
ANDA203002
Marketing category
ANDA
Marketing start
2016-01-18
Marketing end
0000-00-00
Substance
POTASSIUM CHLORIDE
Active strength
10 meq/1
Pharmacologic classes
Increased Large Intestinal Motility [PE], Inhibition Large Intestine Fluid/Electrolyte Absorption [PE], Osmotic Activity [MoA], Osmotic Laxative [EPC], Potassium Compounds [CS], Potassium Salt [EPC]
NDC exclude flag
No
Listing certified through
2023-12-31
Current FDA listing
Historical FDA.report record

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDCDashboard titleSPL versionValidationDashboard ZIP
55154-8089POTASSIUM CHLORIDE CAPSULE, COATED, EXTENDED RELEASE [CARDINAL HEALTH 107, LLC]3Legacy NDC20240912_6ed04120-c734-4316-82eb-2adf4d3593fe.zip

Packages#

Package NDC, 11-digit format, Description table
Package NDC11-digit formatDescriptionUnitsMarketing startMarketing endSampleExclude flagStatus
55154-8089-05515480890010 BLISTER PACK in 1 CARTON (55154-8089-0) > 1 CAPSULE, COATED, EXTENDED RELEASE in 1 BLISTER PACK10 blister pack2016-01-180000-00-00NoNoCurrent