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Sodium Chloride

NDC 0338-0050 · Baxter Healthcare Corporation

Generic nameSodium Chloride
Dosage formSOLUTION
RouteEXTRACORPOREAL
Active ingredient(s)SODIUM CHLORIDE
Strength900 mg/100mL
Pharmacologic classIncreased Large Intestinal Motility [PE], Inhibition Large Intestine Fluid/Electrolyte Absorption [PE], Osmotic Activity [MoA], Osmotic Laxative [EPC]
Marketing categoryNDA

Packages

0338-0050-47 — 4 BAG in 1 CARTON (0338-0050-47) / 3000 mL in 1 BAG

Related Codes

Same active ingredient

FDA lists these products with the same active ingredient.

0264-7800 — Sodium Chloride, 0264-7802 — SODIUM CHLORIDE, 0264-7805 — Sodium Chloride, 0264-7806 — Sodium Chloride, 0264-7865 — SODIUM CHLORIDE and POTASSIUM CHLORIDE, 0264-9375 — Sodium Chloride, 0338-0043 — Sodium Chloride, 0338-0047 — Sodium Chloride, 0338-0048 — sodium chloride, 0338-0049 — Sodium Chloride, 0338-0051 — Sodium Chloride, 0338-0054 — Sodium Chloride, 0338-0056 — Sodium Chloride, 0338-0073 — Dextrose and Sodium Chloride, 0338-0077 — Dextrose and Sodium Chloride, 0338-0085 — Dextrose and Sodium Chloride, 0338-0089 — Dextrose and Sodium Chloride, 0338-0104 — sodium chloride, calcium chloride, potassium chloride,, 0338-0110 — Sodium Chloride, 0338-0114 — sodium chloride, sodium lactate, potassium chloride, calcium 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.