POTASSIUM CHLORIDE

Product NDC
63629-1079
11-digit product format
636291079
Labeler code
63629
Product ID
63629-1079_081a06a9-9d23-4a03-98af-e910cbc6c73e
Type
HUMAN PRESCRIPTION DRUG
Nonproprietary name
POTASSIUM CHLORIDE
Dosage form
CAPSULE, EXTENDED RELEASE
Route
ORAL
Labeler
Bryant Ranch Prepack
Application
ANDA208864
Marketing category
ANDA
Marketing start
2020-01-02
Marketing end
0000-00-00
Substance
POTASSIUM CHLORIDE
Active strength
750 mg/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
63629-1079-1EA - Each63629-1079024e2ffb-2aaf-4b03-8b89-b8faea77a80e12020-09-14
63629-1079-2EA - Each63629-10790a5b3914-0f05-4839-aeb1-bdac79c0e07412020-09-14
63629-1079-3EA - Each63629-1079efab08e5-26b9-4203-99b7-5c72ecfa0d6912020-09-14
63629-1079-4EA - Each63629-10793b4f6fbc-6cc6-4c27-8d85-701b1c3f54a812020-09-14

Packages#

Package NDC, 11-digit format, Description table
Package NDC11-digit formatDescriptionMarketing startMarketing endSampleExclude flagStatus
63629-1079-1636291079011000 CAPSULE, EXTENDED RELEASE in 1 BOTTLE (63629-1079-1) 2020-12-030000-00-00NoNoCurrent
63629-1079-26362910790230 CAPSULE, EXTENDED RELEASE in 1 BOTTLE (63629-1079-2) 2020-11-020000-00-00NoNoCurrent
63629-1079-36362910790390 CAPSULE, EXTENDED RELEASE in 1 BOTTLE (63629-1079-3) 2021-06-140000-00-00NoNoCurrent
63629-1079-463629107904360 CAPSULE, EXTENDED RELEASE in 1 BOTTLE (63629-1079-4) 2021-02-220000-00-00NoNoCurrent