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Potassium Chloride

NDC 0338-0709 · Baxter Healthcare Corporation

Generic namePOTASSIUM CHLORIDE
Dosage formINJECTION, SOLUTION
RouteINTRAVENOUS
Active ingredient(s)POTASSIUM CHLORIDE
Strength7.46 g/1000mL
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 categoryNDA

Packages

0338-0709-48 — 24 BAG in 1 CARTON (0338-0709-48) / 100 mL in 1 BAG

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.

0338-0669 — Potassium Chloride, Dextrose Monohydrate and Sodium Chloride, 0338-0671 — Potassium Chloride, Dextrose Monohydrate and Sodium Chloride, 0338-0673 — Potassium Chloride, Dextrose Monohydrate and Sodium Chloride, 0338-0675 — Potassium Chloride, Dextrose Monohydrate and Sodium Chloride, 0338-0683 — Potassium Chloride and Dextrose Monohydrate, 0338-0691 — Potassium Chloride and Sodium Chloride, 0338-0695 — Potassium Chloride and Sodium Chloride, 0338-0703 — POTASSIUM CHLORIDE, 0338-0704 — Potassium Chloride and Sodium Chloride, 0338-0705 — POTASSIUM CHLORIDE, 0338-0803 — Potassium Chloride, Dextrose Monohydrate and Sodium Chloride, 0338-0807 — Potassium Chloride, Dextrose Monohydrate and Sodium Chloride, 0338-0811 — DEXTROSE MONOHYDRATE, SODIUM CHLORIDE, SODIUM LACTATE, POTASSIUM CHLORIDE, CALCIUM CHLORIDE, 0338-9593 — Sodium Chloride, Sodium Gluconate, Sodium Acetate, Potassium Chloride, Magnesium Chloride, 0378-4560 — potassium chloride, 0378-4561 — potassium chloride, 0404-9936 — Potassium Chloride, 0404-9937 — Potassium Chloride, 0409-5779 — SODIUM CHLORIDE, CALCIUM CHLORIDE, POTASSIUM CHLORIDE, MAGNESIUM CHLORIDE, and SODIUM ACETATE ANHYDROUS, 0409-6635 — 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.