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Potassium Chloride

NDC 51655-568 · Northwind Health Company, LLC

Generic namepotassium chloride
Dosage formTABLET, EXTENDED RELEASE
RouteORAL
Active ingredient(s)POTASSIUM CHLORIDE
Strength1500 mg/1
Pharmacologic classIncreased Large Intestinal Motility [PE], Inhibition Large Intestine Fluid/Electrolyte Absorption [PE], Osmotic Activity [MoA], Osmotic Laxative [EPC], Potassium Compounds [CS], Potassium Salt [EPC]
Marketing categoryANDA

Packages

51655-568-25 — 60 TABLET, EXTENDED RELEASE in 1 BOTTLE, PLASTIC (51655-568-25)

51655-568-26 — 90 TABLET, EXTENDED RELEASE in 1 BOTTLE, PLASTIC (51655-568-26)

51655-568-52 — 30 TABLET, EXTENDED RELEASE in 1 BOTTLE, PLASTIC (51655-568-52)

51655-568-90 — 45 TABLET, EXTENDED RELEASE in 1 BOTTLE, PLASTIC (51655-568-90)

Related Codes

Same active ingredient

FDA lists these products with the same active ingredient.

50090-7639 — Potassium Chloride, 50090-7640 — Potassium Chloride, 50090-7748 — Potassium Chloride, 50090-7749 — Potassium Chloride, 50090-8020 — Polyethylene Glycol 3350, Sodium Sulfate Anhydrous, Sodium Bicarbonate, Sodium Chloride, Potassium Chloride, 50268-671 — Potassium Chloride, 50268-674 — Potassium Chloride, 50268-675 — Potassium Chloride, 51655-226 — Potassium Chloride, 51655-463 — Potassium Chloride, 51655-706 — Potassium Chloride, 51662-1387 — POTASSIUM CHLORIDE, 51662-1421 — POTASSIUM CHLORIDE, 51662-1516 — SODIUM CHLORIDE, SODIUM LACTATE, POTASSIUM CHLORIDE, CALCIUM CHLORIDE, 51662-1521 — SODIUM CHLORIDE, SODIUM LACTATE, POTASSIUM CHLORIDE, CALCIUM CHLORIDE, AND DEXTROSE MONOHYDRATE, 52268-100 — Polyethylene Glycol 3350, Sodium Sulfate Anhydrous, Sodium Bicarbonate, Sodium Chloride, Potassium Chloride, 52268-201 — sodium sulfate, magnesium sulfate, and potassium chloride, 52536-236 — Polyethylene Glycol 3350, Sodium Sulfate Anhydrous, Sodium Bicarbonate, Sodium Chloride, Potassium Chloride, 52536-302 — polyethylene glycol 3350, sodium chloride, sodium bicarbonate, potassium chloride, 53041-420 — Potassium Chloride, +445 more

From the FDA National Drug Code Directory, retrieved August 24, 2026. Product listings are submitted by labelers; FDA does not verify them.