Sodium Chloride

NDC 0990-7730 · ICU Medical Inc.

Generic nameSODIUM CHLORIDE

Dosage formINJECTION, SOLUTION

RouteINTRAVENOUS

Active ingredient(s)SODIUM CHLORIDE

Strength450 mg/100mL

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

Marketing categoryNDA

Packages

0990-7730-36 — 20 POUCH in 1 CASE (0990-7730-36) / 4 BAG in 1 POUCH / 50 mL in 1 BAG

0990-7730-37 — 20 POUCH in 1 CASE (0990-7730-37) / 4 BAG in 1 POUCH / 100 mL in 1 BAG

Related Codes

Same active ingredient

FDA lists these products with the same active ingredient.

0942-9601 — Platelet Additive 3, 0942-9602 — Platelet Additive 3, 0942-9603 — Solucion aditiva para plaquetas 3, 0942-9605 — Platelet Additive 3, 0990-7107 — DEXTROSE MONOHYDRATE, SODIUM CHLORIDE, and POTASSIUM CHLORIDE, 0990-7109 — DEXTROSE MONOHYDRATE, SODIUM CHLORIDE, and POTASSIUM CHLORIDE, 0990-7111 — POTASSIUM CHLORIDE, SODIUM CHLORIDE, CALCIUM CHLORIDE, SODIUM LACTATE, and DEXTROSE MONOHYDRATE, 0990-7115 — SODIUM CHLORIDE and POTASSIUM CHLORIDE, 0990-7116 — SODIUM CHLORIDE and POTASSIUM CHLORIDE, 0990-7670 — SODIUM CHLORIDE, SODIUM ACETATE ANHYDROUS, SODIUM GLUCONATE, POTASSIUM CHLORIDE, AND MAGNESIUM CHLORIDE, 0990-7828 — SODIUM CHLORIDE, SODIUM LACTATE, POTASSIUM CHLORIDE, and CALCIUM CHLORIDE, 0990-7901 — DEXTROSE MONOHYDRATE, SODIUM CHLORIDE, and POTASSIUM CHLORIDE, 0990-7902 — DEXTROSE MONOHYDRATE, SODIUM CHLORIDE, and POTASSIUM CHLORIDE, 0990-7903 — DEXTROSE MONOHYDRATE, SODIUM CHLORIDE, and POTASSIUM CHLORIDE, 0990-7904 — DEXTROSE MONOHYDRATE, SODIUM CHLORIDE, and POTASSIUM CHLORIDE, 0990-7924 — DEXTROSE MONOHYDRATE and SODIUM CHLORIDE, 0990-7925 — DEXTROSE MONOHYDRATE and SODIUM CHLORIDE, 0990-7926 — DEXTROSE MONOHYDRATE and SODIUM CHLORIDE, 0990-7929 — SODIUM CHLORIDE, SODIUM LACTATE, POTASSIUM CHLORIDE, CALCIUM CHLORIDE, and DEXTROSE MONOHYDRATE, 0990-7941 — DEXTROSE MONOHYDRATE and SODIUM CHLORIDE, +1000 more

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