NDC 24979-230 – Potassium Chloride

Potassium Chloride 750 mg/1 · Tablet, Extended Release · Oral

Human Prescription Drug

Product NDC24979-230

Product details

Brand name
Potassium Chloride
Generic name
Potassium Chloride
Labeler
Upsher-Smith Laboratories, LLC
Dosage form
Tablet, Extended Release
Route
Oral
Marketing category
ANDA · ANDA218979
Marketed since
October 28, 2024
Listing expires
December 31, 2026
Pharmacologic class
Osmotic Laxative; Potassium Salt

Active ingredients

Uses, dosage, side effects and warnings for Potassium Chloride →

Package NDC codes (3)

Package NDCDescriptionSince
24979-230-0064000 TABLET, EXTENDED RELEASE in 1 DRUM (24979-230-00)Jun 1, 2025
24979-230-01100 TABLET, EXTENDED RELEASE in 1 BOTTLE (24979-230-01)Oct 28, 2024
24979-230-031000 TABLET, EXTENDED RELEASE in 1 BOTTLE (24979-230-03)Oct 28, 2024

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