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SODIUM CHLORIDE

NDC 0338-9659 · Baxter Healthcare Corporation

Generic namesodium chloride
Dosage formINJECTION, SOLUTION
RouteINTRAVENOUS
Active ingredient(s)SODIUM CHLORIDE
Strength9 g/1000mL
Pharmacologic classIncreased Large Intestinal Motility [PE], Inhibition Large Intestine Fluid/Electrolyte Absorption [PE], Osmotic Activity [MoA], Osmotic Laxative [EPC]
Marketing categoryNDA

Packages

0338-9659-75 — 50 mL in 1 BAG (0338-9659-75)

Related Codes

Same active ingredient

FDA lists these products with the same active ingredient.

0338-0695 — Potassium Chloride and Sodium Chloride, 0338-0704 — Potassium Chloride and Sodium Chloride, 0338-0803 — Potassium Chloride, Dextrose Monohydrate and Sodium Chloride, 0338-0807 — Potassium Chloride, Dextrose Monohydrate and Sodium Chloride, 0338-0811 — DEXTROSE MONOHYDRATE, SODIUM CHLORIDE, SODIUM LACTATE, POTASSIUM CHLORIDE, CALCIUM CHLORIDE, 0338-9151 — sodium chloride, 0338-9159 — sodium chloride, 0338-9543 — sodium chloride, 0338-9593 — Sodium Chloride, Sodium Gluconate, Sodium Acetate, Potassium Chloride, Magnesium Chloride, 0338-9657 — sodium chloride, 0338-9660 — sodium chloride, 0338-9661 — sodium chloride, 0338-9662 — sodium chloride, 0338-9663 — sodium chloride, 0338-9791 — Sodium Chloride, 0338-9793 — Sodium Chloride, 0338-9799 — Dextrose Anhydrous and Sodium Chloride, 0338-9804 — Sodium Chloride, 0338-9806 — Sodium Chloride, 0338-9808 — Sodium Chloride, +526 more

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