Sodium Chloride

NDC 0641-6144 · Hikma Pharmaceuticals USA Inc.

Generic nameSodium Chloride

Dosage formINJECTION

RouteINTRAMUSCULAR, INTRAVENOUS, SUBCUTANEOUS

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

0641-6144-25 — 25 VIAL in 1 CARTON (0641-6144-25) / 10 mL in 1 VIAL (0641-6144-01)

Related Codes

Same active ingredient

FDA lists these products with the same active ingredient.

0409-1966 — SODIUM CHLORIDE, 0409-4888 — Sodium Chloride, 0409-5779 — SODIUM CHLORIDE, CALCIUM CHLORIDE, POTASSIUM CHLORIDE, MAGNESIUM CHLORIDE, and SODIUM ACETATE ANHYDROUS, 0409-6660 — SODIUM CHLORIDE, 0409-7101 — Sodium Chloride, 0409-7969 — POTASSIUM CHLORIDE, SODIUM CHLORIDE, CALCIUM CHLORIDE, and MAGNESIUM CHLORIDE, 0487-4301 — Sodium Chloride, 0536-1253 — sodium chloride, 0536-1254 — sodium chloride, 0641-0497 — Sodium Chloride, 0941-0409 — sodium chloride, sodium lactate, calcium chloride, magnesium chloride and dextrose, 0941-0411 — sodium chloride, sodium lactate, calcium chloride, magnesium chloride and dextrose, 0941-0413 — sodium chloride, sodium lactate, calcium chloride, magnesium chloride and dextrose, 0941-0415 — sodium chloride, sodium lactate, calcium chloride, magnesium chloride and dextrose, 0941-0424 — sodium chloride, sodium lactate, calcium chloride, magnesium chloride and dextrose, 0941-0426 — sodium chloride, sodium lactate, calcium chloride, magnesium chloride and dextrose, 0941-0427 — sodium chloride, sodium lactate, calcium chloride, magnesium chloride and dextrose, 0941-0429 — sodium chloride, sodium lactate, calcium chloride, magnesium chloride and dextrose, 0941-0430 — sodium chloride, sodium lactate, calcium chloride, magnesium chloride and dextrose, 0941-0433 — sodium chloride, sodium lactate, calcium chloride, magnesium chloride and dextrose, +526 more

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