POTASSIUM CHLORIDE

Product NDC
70518-3384
11-digit product format
705183384
Labeler code
70518
Product ID
70518-3384_d9f1db05-4113-2a8f-e053-2a95a90ae0b2
Type
HUMAN PRESCRIPTION DRUG
Nonproprietary name
POTASSIUM CHLORIDE
Dosage form
CAPSULE, EXTENDED RELEASE
Route
ORAL
Labeler
REMEDYREPACK INC.
Application
ANDA208864
Marketing category
ANDA
Marketing start
2022-03-10
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 Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDCDashboard titleSPL versionValidationDashboard ZIP
70518-3384POTASSIUM CHLORIDE CAPSULE, EXTENDED RELEASE [REMEDYREPACK INC.]3Legacy NDC20240316_b39640f1-c851-4f69-a280-4c6fdd97847b.zip

Packages#

Package NDC, 11-digit format, Description table
Package NDC11-digit formatDescriptionUnitsMarketing startMarketing endSampleExclude flagStatus
70518-3384-070518338400100 POUCH in 1 BOX (70518-3384-0) > 1 CAPSULE, EXTENDED RELEASE in 1 POUCH (70518-3384-1) 100 pouch2022-03-100000-00-00NoNoCurrent