Dextrose

NDC 65219-234 · Fresenius Kabi USA, LLC

Generic nameDextrose Monohydrate

Dosage formINJECTION, SOLUTION

RouteINTRAVENOUS

Active ingredient(s)DEXTROSE MONOHYDRATE

Strength2500 mg/50mL

Marketing categoryANDA

Packages

65219-234-10 — 60 BAG in 1 CASE (65219-234-10) / 50 mL in 1 BAG (65219-234-01)

Related Codes

Same active ingredient

FDA lists these products with the same active ingredient.

63323-874 — DEXTROSE MONOHYDRATE, SODIUM 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, 65219-153 — DEXTROSE MONOHYDRATE, SODIUM CHLORIDE, and POTASSIUM CHLORIDE, 65219-236 — Dextrose Monohydrate, 65219-238 — Dextrose Monohydrate, 65219-240 — Dextrose Monohydrate, 65219-241 — SODIUM CHLORIDE, SODIUM LACTATE, POTASSIUM CHLORIDE, CALCIUM CHLORIDE, and DEXTROSE MONOHYDRATE, 65219-243 — SODIUM CHLORIDE, SODIUM LACTATE, POTASSIUM CHLORIDE, CALCIUM CHLORIDE, and DEXTROSE MONOHYDRATE, 65219-246 — POTASSIUM CHLORIDE, SODIUM CHLORIDE, CALCIUM CHLORIDE, SODIUM LACTATE, and DEXTROSE MONOHYDRATE, 65219-456 — Dextrose Monohydrate, 65219-458 — Dextrose Monohydrate, 65219-460 — Dextrose Monohydrate, 65219-462 — Dextrose Monohydrate, +193 more

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