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Dextrose

NDC 65219-464 · FRESENIUS KABI USA, LLC

Generic nameDextrose Monohydrate
Dosage formINJECTION, SOLUTION
RouteINTRAVENOUS
Active ingredient(s)DEXTROSE MONOHYDRATE
Strength50 mg/mL
Marketing categoryANDA

Packages

65219-464-50 — 50 BAG in 1 CASE (65219-464-50) / 100 mL in 1 BAG (65219-464-05)

Related Codes

Same active ingredient

FDA lists these products with the same active ingredient.

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, 70518-4219 — DEXTROSE MONOHYDRATE, 70518-4452 — Dextrose monohydrate, 71872-7003 — DEXTROSE MONOHYDRATE, 71872-7057 — DEXTROSE MONOHYDRATE, 71872-7102 — DEXTROSE MONOHYDRATE, 71872-7214 — Dextrose monohydrate, 71872-7282 — Dextrose Monohydrate, 76329-3302 — Dextrose Monohydrate, 79403-791 — Sterile Cord Blood Collection Unit, 84549-460 — Dextrose Monohydrate, +185 more

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