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Sodium Chloride

NDC 63323-632 · Fresenius Kabi USA, LLC

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

Packages

63323-632-40 — 10 BAG in 1 CASE (63323-632-40) / 1000 mL in 1 BAG (63323-632-10)

63323-632-75 — 20 BAG in 1 CASE (63323-632-75) / 500 mL in 1 BAG (63323-632-20)

Related Codes

Same active ingredient

FDA lists these products with the same active ingredient.

63323-088 — Sodium Chloride, 63323-090 — Sodium Chloride, 63323-093 — Sodium Chloride, 63323-095 — Sodium Chloride, 63323-099 — Sodium Chloride, 63323-164 — SODIUM CHLORIDE, SODIUM LACTATE, POTASSIUM CHLORIDE, CALCIUM CHLORIDE, 63323-186 — SODIUM CHLORIDE, 63323-530 — Sodium Chloride, 63323-623 — SODIUM CHLORIDE, 63323-626 — SODIUM CHLORIDE, 63323-683 — Sodium Chloride and Potassium Chloride, 63323-686 — Sodium Chloride and Potassium Chloride, 63323-688 — Sodium Chloride and Potassium Chloride, 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, 63323-874 — DEXTROSE MONOHYDRATE, SODIUM CHLORIDE, 63323-924 — SODIUM CHLORIDE, 63941-704 — Nasal, +526 more

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