DEXTROSE AND SODIUM CHLORIDE

NDC 63323-874 · Fresenius Kabi USA, LLC

Generic nameDEXTROSE MONOHYDRATE, SODIUM CHLORIDE

Dosage formINJECTION, SOLUTION

RouteINTRAVENOUS

Active ingredient(s)DEXTROSE MONOHYDRATE, SODIUM CHLORIDE

Strength2.5; .45 g/100mL; g/100mL

Pharmacologic classIncreased Large Intestinal Motility [PE], Inhibition Large Intestine Fluid/Electrolyte Absorption [PE], Osmotic Activity [MoA], Osmotic Laxative [EPC]

Marketing categoryANDA

Packages

63323-874-10 — 10 BAG in 1 CASE (63323-874-10) / 1000 mL in 1 BAG

Related Codes

Same active ingredient

FDA lists these products with the same active ingredient.

63323-667 — Potassium Chloride, Dextrose Monohydrate, 63323-669 — Potassium Chloride, Dextrose Monohydrate, 63323-683 — Sodium Chloride and Potassium Chloride, 63323-686 — Sodium Chloride and Potassium Chloride, 63323-688 — Sodium Chloride and Potassium Chloride, 63323-824 — Dextrose Monohydrate, 63323-867 — DEXTROSE MONOHYDRATE and SODIUM CHLORIDE, 63323-869 — DEXTROSE MONOHYDRATE and SODIUM CHLORIDE, 63323-870 — DEXTROSE MONOHYDRATE and SODIUM CHLORIDE, 63323-873 — DEXTROSE MONOHYDRATE and SODIUM CHLORIDE, 63323-924 — SODIUM CHLORIDE, 63479-0705 — ADENOSINE TRIPHOSPHATE, IGNATIA AMARA, KALI PHOSPHORICUM, NATRUM MURIATICUM, NUX VOMICA, SULPHUR, 63479-2505 — ADENOSINE TRIPHOSPHATE, IGNATIA AMARA, KALI PHOSPHORICUM, NATRUM MURIATICUM, NUX VOMICA, SULPHUR, 63941-704 — Nasal, 64253-202 — SODIUM CHLORIDE, 64380-765 — Polyethylene Glycol 3350 and electrolytes - Unflavored, 64380-766 — Polyethylene Glycol 3350 and electrolytes with Lemon Flavor, 64380-767 — Polyethylene Glycol 3350 and electrolytes with Orange Flavor, 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, +675 more

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