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POTASSIUM CHLORIDE

NDC 31722-135 · Camber Pharmaceuticals, Inc.

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

31722-135-01 — 100 TABLET, EXTENDED RELEASE in 1 BOTTLE (31722-135-01)

31722-135-05 — 500 TABLET, EXTENDED RELEASE in 1 BOTTLE (31722-135-05)

Related Codes

Same active ingredient

FDA lists these products with the same active ingredient.

24338-236 — Polyethylene Glycol 3350, Sodium Sulfate Anhydrous, Sodium Bicarbonate, Sodium Chloride, Potassium Chloride, 24571-117 — magnesium chloride, sodium chloride, sodium bicarbonate, potassium chloride, and sodium phosphate dibasic dihydrate, 24979-229 — Potassium Chloride, 24979-230 — Potassium Chloride, 24979-231 — Potassium Chloride, 24979-232 — Potassium Chloride, 27808-168 — Potassium Chloride, 27808-169 — Potassium Chloride, 31722-133 — Potassium CHLORIDE, 31722-134 — Potassium Chloride, 31722-494 — potassium chloride, 31722-495 — potassium chloride, 33342-417 — Potassium chloride, 33342-418 — Potassium chloride, 33342-511 — Potassium Chloride, 33342-512 — Potassium Chloride, 34666-406 — Echinacea, Ferrum phosphoricum, Kali muriaticum, Zincum gluconicum, 37662-0883 — Kali Muriaticum, 37662-0884 — Kali Muriaticum, 37662-0885 — Kali Muriaticum, +445 more

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