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POTASSIUM CHLORIDE

NDC 65219-008 · Fresenius Kabi USA, LLC

Generic namePOTASSIUM CHLORIDE
Dosage formINJECTION
RouteINTRAVENOUS
Active ingredient(s)POTASSIUM CHLORIDE
Strength20 meq/50mL
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

65219-008-51 — 60 BAG in 1 CARTON (65219-008-51) / 50 mL in 1 BAG (65219-008-50)

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.

64380-768 — Polyethylene Glycol 3350, Sodium Chloride, Sodium Bicarbonate and Potassium Chloride - Unflavored, 64380-769 — Polyethylene Glycol 3350, Sodium Chloride, Sodium Bicarbonate and Potassium Chloride with Lemon Flavor, 64380-770 — Polyethylene Glycol 3350, Sodium Chloride, Sodium Bicarbonate and Potassium Chloride with Orange Flavor, 64380-860 — Potassium Chloride, 64380-861 — Potassium Chloride, 64380-875 — Potassium Chloride, 64950-320 — Potassium Chloride, 64950-321 — Potassium Chloride, 65219-004 — POTASSIUM CHLORIDE, 65219-006 — POTASSIUM CHLORIDE, 65219-010 — POTASSIUM CHLORIDE, 65219-012 — POTASSIUM CHLORIDE, 65219-118 — DEXTROSE MONOHYDRATE, SODIUM CHLORIDE, and POTASSIUM CHLORIDE, 65219-119 — DEXTROSE MONOHYDRATE, SODIUM CHLORIDE, and POTASSIUM CHLORIDE, 65219-142 — DEXTROSE MONOHYDRATE, SODIUM CHLORIDE, and POTASSIUM CHLORIDE, 65219-144 — DEXTROSE MONOHYDRATE, SODIUM CHLORIDE, and POTASSIUM CHLORIDE, 65219-146 — DEXTROSE MONOHYDRATE, SODIUM CHLORIDE, and POTASSIUM CHLORIDE, 65219-148 — DEXTROSE MONOHYDRATE, SODIUM CHLORIDE, and POTASSIUM CHLORIDE, 65219-150 — DEXTROSE MONOHYDRATE, SODIUM CHLORIDE, and POTASSIUM CHLORIDE, 65219-151 — DEXTROSE MONOHYDRATE, SODIUM CHLORIDE, and 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.