Potassium Chloride

Product NDC
0904-6930
11-digit product format
009046930
Labeler code
0904
Product ID
0904-6930_4eda7e05-fbe6-4a4a-be1e-41bb73d50c43
Type
HUMAN PRESCRIPTION DRUG
Nonproprietary name
Potassium Chloride
Dosage form
CAPSULE, COATED, EXTENDED RELEASE
Route
ORAL
Labeler
Major Pharmaceuticals
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 Billing Units#

Package NDC, Billing unit, Product NDC table
Package NDCBilling unitProduct NDCDailyMed indexing SPLSPL versionEffective
0904-6930-61EA - Each0904-69304040a82e-fc32-40bd-901e-270442f2feac12020-03-10

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDCDashboard titleSPL versionValidationDashboard ZIP
0904-6930POTASSIUM CHLORIDE CAPSULE, COATED, EXTENDED RELEASE [MAJOR PHARMACEUTICALS]3Legacy NDC20240703_4732f78f-ed64-4278-9a6a-8f248c37c036.zip

Packages#

Package NDC, 11-digit format, Description table
Package NDC11-digit formatDescriptionUnitsMarketing startMarketing endSampleExclude flagStatus
0904-6930-6100904693061100 BLISTER PACK in 1 CARTON (0904-6930-61) > 1 CAPSULE, COATED, EXTENDED RELEASE in 1 BLISTER PACK100 blister pack2016-01-180000-00-00NoNoCurrent