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Potassium Chloride

NDC 14789-107 · Nexus Pharamaceuticals Inc.

Generic namePotassium Chloride
Dosage formINJECTION
RouteINTRAVENOUS
Active ingredient(s)POTASSIUM CHLORIDE
Strength29.8 mg/mL
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

14789-107-05 — 24 BAG in 1 BOX (14789-107-05) / 50 mL in 1 BAG (14789-107-08)

14789-107-10 — 24 BAG in 1 BOX (14789-107-10) / 100 mL in 1 BAG (14789-107-16)

Billed under HCPCS

J3480 — Injection, potassium chloride, per 2 meq Medicare Part B payment limit (ASP + 6%): $0.14

Related Codes

Same active ingredient

FDA lists these products with the same active ingredient.

0990-7967 — SODIUM CHLORIDE, SODIUM ACETATE ANHYDROUS, SODIUM GLUCONATE, POTASSIUM CHLORIDE, AND MAGNESIUM CHLORIDE, 0990-7968 — Dextrose, Sodium Chloride, Sodium Acetate Anhydrous, Sodium Gluconate, Potassium Chloride, and Magnesium Chloride, 0990-7982 — SODIUM CHLORIDE, POTASSIUM CHLORIDE, AND CALCIUM CHLORIDE, 0990-7993 — DEXTROSE MONOHYDRATE, SODIUM CHLORIDE, and POTASSIUM CHLORIDE, 0990-9257 — SODIUM CHLORIDE and POTASSIUM CHLORIDE, 10135-807 — Potassium Chloride for Oral Solution, 10135-819 — Potassium Chloride for Oral Solution, 10135-820 — Potassium Chloride for Oral Solution, 10572-100 — Polyethylene Glycol 3350, Sodium Sulfate Anhydrous, Sodium Bicarbonate, Sodium Chloride, Potassium Chloride, 10572-302 — polyethylene glycol 3350, sodium chloride, sodium bicarbonate, potassium chloride, 14789-108 — Potassium Chloride, 14789-109 — Potassium Chloride, 15370-305 — Potassium Chloride, 15370-306 — potassium chloride, 15370-307 — potassium chloride, 15631-0251 — KALI MURIATICUM, 15631-2802 — KALI MUR, 16571-842 — potassium chloride, 16571-843 — potassium chloride, 16714-824 — Potassium Chloride, +599 more

From the FDA National Drug Code Directory, retrieved 2026-08-24. Product listings are submitted by labelers; FDA does not verify them.