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Potassium Chloride in Dextrose and Sodium Chloride

NDC 65219-118 · Fresenius Kabi USA, LLC

Generic nameDEXTROSE MONOHYDRATE, SODIUM CHLORIDE, and POTASSIUM CHLORIDE
Dosage formINJECTION, SOLUTION
RouteINTRAVENOUS
Active ingredient(s)DEXTROSE MONOHYDRATE, SODIUM CHLORIDE, POTASSIUM CHLORIDE
Strength50; 1.49; 9 g/1000mL; g/1000mL; g/1000mL
Pharmacologic classIncreased Large Intestinal Motility [PE], Increased Large Intestinal Motility [PE], Inhibition Large Intestine Fluid/Electrolyte Absorption [PE], Inhibition Large Intestine Fluid/Electrolyte Absorption [PE], Osmotic Activity [MoA], Osmotic Activity [MoA], Osmotic Laxative [EPC], Osmotic Laxative [EPC], Potassium Compounds [CS], Potassium Salt [EPC]
Marketing categoryANDA

Packages

65219-118-10 — 10 BAG in 1 CASE (65219-118-10) / 1000 mL in 1 BAG (65219-118-01)

Related Codes

Same active ingredient

FDA lists these products with the same active ingredient.

64578-0096 — Carduus Marianus, Chelidonium Majus, Echinacea (Angustifolia), Glandula Suprarenalis Suis, Natrum Muriaticum, Phosphoricum Acidum,…, 64616-045 — Ear Drops, 64616-050 — Ear Drops, 64950-320 — Potassium Chloride, 64950-321 — Potassium Chloride, 65219-004 — POTASSIUM CHLORIDE, 65219-006 — POTASSIUM CHLORIDE, 65219-008 — POTASSIUM CHLORIDE, 65219-010 — POTASSIUM CHLORIDE, 65219-012 — 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, 65219-153 — DEXTROSE MONOHYDRATE, SODIUM CHLORIDE, and POTASSIUM CHLORIDE, 65219-218 — SODIUM CHLORIDE, 65219-220 — SODIUM CHLORIDE, +1185 more

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

Read from: FDA National Drug Code Directory, product.txt and package.txt (accessdata.fda.gov/cder/ndctext.zip) — Snapshot retrieved 2026-08-24, loaded 2026-08-24; CMS Medicare Part B Drug Average Sales Price (ASP) Pricing Files (cms.gov/medicare/payment/part-b-drugs/asp-pricing-files) -- the NDC-HCPCS crosswalk and Part B payment limit files — 2026 Q3 (July 2026 release). All data sources · How to read the labels