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POTASSIUM CHLORIDE

NDC 72189-027 · Direct_Rx

Generic namePOTASSIUM CHLORIDE
Dosage formTABLET, EXTENDED RELEASE
RouteORAL
Active ingredient(s)POTASSIUM CHLORIDE
Strength750 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

72189-027-04 — 4 TABLET, EXTENDED RELEASE in 1 BOTTLE (72189-027-04)

72189-027-30 — 30 TABLET, EXTENDED RELEASE in 1 BOTTLE (72189-027-30)

Related Codes

Same active ingredient

FDA lists these products with the same active ingredient.

71610-944 — Potassium Chloride, 71610-945 — Potassium Chloride, 71610-960 — Potassium Chloride, 71610-977 — Potassium Chloride, 71656-021 — POTASSIUM CHLORIDE ORAL, 71656-022 — POTASSIUM CHLORIDE, 71919-813 — POTASSIUM CHLORIDE, 72162-1076 — POTASSIUM CHLORIDE, 72162-1786 — Potassium Chloride, 72162-2310 — Potassium Chloride, 72189-462 — Potassium Chloride ER, 72189-629 — Potassium Chloride ER, 72189-648 — Potassium Chloride ER, 72603-337 — potassium chloride, 72603-338 — potassium chloride, 72603-407 — Potassium Chloride, 72789-056 — POTASSIUM CHLORIDE, 72789-057 — POTASSIUM CHLORIDE, 72789-365 — Potassium Chloride, 72789-503 — 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.